Organic compound, organic light emitting diode and organic light emitting device including the organic compound

ABSTRACT

The present disclosure relates to an organic compound having the following structure, and an organic light emitting diode (OLED) and an organic light emitting device including the organic compound. Applying the organic compound into an emissive layer makes the OLED and the organic light emitting device lower their driving voltage, improves their luminous efficiency and color purity.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the priority benefit under 35 U.S.C. § 119(a) to Korean Patent Application No. 10-2019-0142232, filed in the Republic of Korea on Nov. 8, 2019, the entire contents of which are incorporated herein by reference into the present application.

BACKGROUND Technical Field

The present disclosure relates to an organic compound, and more specifically, to an organic compound having excellent luminous efficiency and color purity to be applicable into an emissive layer, an organic light emitting diode and an organic light emitting device including the compound.

Discussion of the Related Art

As display devices have become larger, there exists a need for a flat display device with a lower space requirement. Among the flat display devices used widely at present, organic light emitting diodes (OLEDs) are rapidly replacing liquid crystal display devices (LCDs).

In the OLED, when electrical charges are injected into an emitting material layer between an electron injection electrode (i.e., cathode) and a hole injection electrode (i.e., anode), electrical charges are recombined to form excitons, and then emit light as the recombined excitons are shifted to a stable ground state. The OLED can be formed as a thin film having a thickness less than 2000 Å and can be implement unidirectional or bidirectional images as electrode configurations. In addition, OLEDs can be formed on a flexible transparent substrate such as a plastic substrate so that OLED can implement a flexible or foldable display with ease. Moreover, the OLED can be driven at a lower voltage of 10 V or less. Besides, the OLED has relatively lower power consumption for driving compared to plasma display panels and inorganic electroluminescent devices, and the color purity of the OLED is very high. Particularly, the OLED can implement red, green and blue colors, thus it has attracted a lot of attention as a light emitting device.

However, the luminous materials applied into the OLED have not shown satisfactory luminous efficiency. Also, the OLED in which the luminous materials are applied has driven at relatively higher driving voltages, thus it has increased power consumption. In addition, the luminous material applied into the OLED has short luminous lifetime or bad color purity.

SUMMARY

Accordingly, embodiments of the present disclosure are directed to an organic compound and an OLED and an organic light emitting device including the organic compound that substantially obviates one or more of the problems due to the limitations and disadvantages of the related art.

An object of the present disclosure is to provide an organic compound having excellent luminous efficiency and color purity, an OLED and an organic light emitting device into which the organic compound is applied.

Another object of the present disclosure is to provide an organic compound that can be driven at low voltage and reduce power consumption, an OLED and an organic light emitting device having the compound.

Additional features and aspects will be set forth in the description that follows, and in part will be apparent from the description, or may be learned by practice of the inventive concepts provided herein. Other features and aspects of the inventive concept may be realized and attained by the structure particularly pointed out in the written description, or derivable therefrom, and the claims hereof as well as the appended drawings.

To achieve these and other aspects of the inventive concepts, as embodied and broadly described, the present disclosure provides an organic compound having the following structure of Chemical Formula 1:

wherein each of R₁ to R₆ is independently selected from the group consisting of hydrogen, an unsubstituted or substituted C₁-C₂₀ alkyl group, an unsubstituted or substituted C₁-C₂₀ alkoxy group, an unsubstituted or substituted C₁-C₂₀ alkyl amino group, an unsubstituted or substituted C₆-C₃₀ aromatic group and an unsubstituted or substituted C₃-C₃₀ hetero aromatic group, or two adjacent groups among R₁ to R₆ form a C₆-C₂₀ fused aromatic ring or a C₃-C₂₀ fused hetero aromatic ring; each of A₁ to A₄ is independently CR₈ or nitrogen (N), wherein at least one of A₁ to A₄ is nitrogen; each of R₇ and R₈ is independently hydrogen, an unsubstituted or substituted C₁-C₁₀ alkyl group, an unsubstituted or substituted C₆-C₃₀ aromatic group or an unsubstituted or substituted C₃-C₃₀ hetero aromatic group; each of X₁ and X₂ is independently halogen, a nitrile group, a C₁-Cao alkyl group or a C₁-C₂₀ halo alkyl group; and X₃ is oxygen (O) or sulfur (S).

In another aspect, an OLED comprises a first electrode; a second electrode facing the first electrode; and a first emitting material layer disposed between the first and second electrodes, wherein the first emitting material layer comprises the organic compound.

For example, the organic compound may be comprised in the first emitting material layer as a dopant, and the emissive layer may have at least one emitting unit.

In still another aspect, an organic light emitting device comprises a substrate and an OLED disposed over the substrate, as described above.

It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory and are intended to provide further explanation of the inventive concepts as claimed.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings, which are included to provide a further understanding of the disclosure, are incorporated in and constitute a part of this application, illustrate embodiments of the disclosure and together with the description serve to explain principles of the disclosure.

FIG. 1 is a schematic cross-sectional view illustrating an organic light emitting display device in accordance with an aspect of the present disclosure.

FIG. 2 is a schematic cross-sectional view illustrating an OLED in accordance with an exemplary aspect of the present disclosure.

FIG. 3 is a schematic diagram illustrating luminous mechanism by energy level bandgap among luminous materials in accordance with an exemplary aspect of the present disclosure.

FIG. 4 is a schematic cross-sectional view illustrating an OLED in accordance with another exemplary aspect of the present disclosure.

FIG. 5 is a schematic diagram illustrating a luminous mechanism of a delayed fluorescent material.

FIG. 6 is a schematic diagram illustrating luminous mechanism by energy level bandgap among luminous materials in accordance with another exemplary aspect of the present disclosure.

FIG. 7 is a schematic cross-sectional view illustrating an OLED diode in accordance with another exemplary aspect of the present disclosure.

FIG. 8 is a schematic diagram illustrating luminous mechanism by energy level bandgap among luminous materials in accordance with another exemplary aspect of the present disclosure.

FIG. 9 is a schematic cross-sectional view illustrating an OLED in accordance with another exemplary aspect of the present disclosure.

FIG. 10 is a schematic diagram illustrating luminous mechanism by energy level bandgap among luminous materials in accordance with another exemplary aspect of the present disclosure.

DETAILED DESCRIPTION

Reference and discussions will now be made below in detail to aspects, embodiments and examples of the disclosure, some examples of which are illustrated in the accompanying drawings.

[Organic Compound]

An organic compound applied to an organic light emitting diode (OLED) should have excellent luminous properties and luminous lifetime. In addition, in an EML applying a host-dopant system, the dopant should have been designed to receive efficiently exciton energies generated in the host. An organic compound in accordance with the present disclosure satisfies the above-described requirements and may have the following structure of Chemical Formula 1:

In Chemical Formula 1, each of R₁ to R₆ is independently selected from the group consisting of hydrogen, an unsubstituted or substituted C₁-C₂₀ alkyl group, an unsubstituted or substituted C₁-C₂₀ alkoxy group, an unsubstituted or substituted C₁-C₂₀ alkyl amino group, an unsubstituted or substituted C₆-C₃₀ aromatic group and an unsubstituted or substituted C₃-C₃₀ hetero aromatic group, or two adjacent groups among R₁ to R₆ form a C₆-C₂₀ fused aromatic ring or a C₃-C₂₀ fused hetero aromatic ring; each of A₁ to A₄ is independently CR₈ or nitrogen (N), wherein at least one of A₁ to A₄ is nitrogen; each of R₇ and R₈ is independently hydrogen, an unsubstituted or substituted C₁-C₁₀ alkyl group, an unsubstituted or substituted C₆-C₃₀ aromatic group or an unsubstituted or substituted C₃-C₃₀ hetero aromatic group; each of X₁ and X₂ is independently halogen, a nitrile group, a C₁-C₂₀ alkyl group or a C₁-C₂₀ halo alkyl group; and X₃ is oxygen (O) or sulfur (S).

As used herein, the term ‘unsubstituted” means that hydrogen is linked, and in this case, hydrogen comprises protium, deuterium and tritium.

As used herein, the substituent in the term “substituted” comprises, but is not limited to, unsubstituted or halogen-substituted C₁-C₂₀ alkyl, unsubstituted or halogen-substituted C₁-C₂₀ alkoxy, halogen, cyano, —CF₃, a hydroxyl group, a carboxylic group, a carbonyl group, an amino group, a C₁-C₁₀ alkyl amino group, a C₆-C₃₀ aryl amino group, a C₃-C₃₀ hetero aryl amino group, a C₆-C₃₀ aryl group, a C₃-C₃₀ hetero aryl group, a nitro group, a hydrazyl group, a sulfonate group, a C₁-C₂₀ alkyl silyl group, a C₆-C₃₀ aryl silyl group and a C₃-C₃₀ hetero aryl silyl group.

As used herein, the term ‘hetero” in such as “a hetero aromatic ring”, “a hetero cycloalkyene group”, “a hetero arylene group”, “a hetero aryl alkylene group”, “a hetero aryl oxylene group”, “a hetero cycloalkyl group”, “a hetero aryl group”, “a hetero aryl alkyl group”, “a hetero aryloxyl group”, “a hetero aryl amino group” means that at least one carbon atom, for example 1-5 carbons atoms, constituting an aromatic ring or an alicyclic ring is substituted with at least one hetero atom selected from the group consisting of N, O, S, P and combination thereof.

In one exemplary aspect, the C₆-C₃₀ aromatic group in each of R₁ to R₈ may comprise a C₆-C₃₀ aryl group, a C₇-C₃₀ aryl alkyl group, a C₆-C₃₀ aryloxyl group and a C₆-C₃₀ aryl amino group. The C₃-C₃₀ hetero aromatic group in each of R₁ to R₈ may comprise a C₃-C₃₀ hetero aryl group, a C₄-C₃₀ hetero aryl alkyl group, a C₃-C₃₀ hetero aryloxyl group and a C₃-C₃₀ hetero aryl amino group.

In one exemplary aspect, the C₆-C₃₀ aryl group in each of R₁ to R₈ or substituted to R₁ to R₈ may comprise independently, but is not limited to, an unfused or fused aryl group such as phenyl, biphenyl, terphenyl, naphthyl, anthracenyl, pentalenyl, indenyl, indeno-indenyl, heptalenyl, biphenylenyl, indacenyl, phenalenyl, phenanthrenyl, benzo-phenanthrenyl, dibenzo-phenanthrenyl, azulenyl, pyrenyl, fluoranthenyl, triphenylenyl, chrysenyl, tetraphenylenyl, tetracenyl, pleiadenyl, picenyl, pentaphenylenyl, pentacenyl, fluorenyl, indeno-fluorenyl and spiro-fluorenyl.

In another exemplary aspect, the C₃-C₃₀ hetero aryl group in each of R₁ to R₈ or substituted to R₁ to R₈ may comprise independently, but is not limited to, an unfused or fused hetero aryl group such as pyrrolyl, pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, triazinyl, tetrazinyl, imidazolyl, pyrazolyl, indolyl, iso-indolyl, indazolyl, indolizinyl, pyrrolizinyl, carbazolyl, benzo-carbazolyl, dibenzo-carbazolyl, indolo-carbazolyl, indeno-carbazolyl, benzo-furo-carbazolyl, benzo-thieno-carbazolyl, carbolinyl, quinolinyl, iso-quinolinyl, phthlazinyl, quinoxalinyl, cinnolinyl, quinazolinyl, quinolizinyl, purinyl, benzo-quinolinyl, benzo-iso-quinolinyl, benzo-quinazolinyl, benzo-quinoxalinyl, acridinyl, phenazinyl, phenoxazinyl, phenothiazinyl, phenanthrolinyl, perimidinyl, phenanthridinyl, pteridinyl, naphthyridinyl, furanyl, pyranyl, oxazinyl, oxazolyl, oxadiazolyl, triazolyl, dioxinyl, benzo-furanyl, dibenzo-furanyl, thiopyranyl, xanthenyl, chromenyl, iso-chromenyl, thioazinyl, thiophenyl, benzo-thiophenyl, dibenzo-thiophenyl, difuro-pyrazinyl, benzofuro-dibenzo-furanyl, benzothieno-benzo-thiophenyl, benzothieno-dibenzo-thiophenyl, benzothieno-benzo-furanyl, benzothieno-dibenzo-furanyl, xanthne-linked spiro acridinyl, dihydroacridinyl substituted with at least one C₁-C₁₀ alkyl and N-substituted spiro fluorenyl.

The organic compound having the structure of Chemical Formula 1 comprises a boron-dipyrromethene (BODIPY) moiety and a fused hetero aromatic moiety including at least one nitrogen atom and an oxygen or a sulfur. The BODIPY moiety and the fused hetero aromatic moiety have relatively small plate-like structures, thus there exist less overlapping regions among the adjacent molecules. In addition, as the organic compound includes at least one group substituted directly to the BODIPY moiety, the distance among adjacent molecules increases.

The exciton energy among the luminous material may be transferred by Dexter transfer mechanism and FRET (Forster resonance energy transfer) mechanism. In FRET mechanism, only singlet exciton energy is transferred non-radiatively through electrical field caused by dipole-dipole interaction. On the contrary, triplet exciton energy as well as singlet exciton energy is transferred via Dexter energy transfer mechanism with exchanging directly electrons among the luminous materials. The molecules should be adjacently disposed less than 10 Å in order to transfer exciton energy in Dexter energy transfer mechanism.

When the organic compound having the structure of Chemical Formula 1 is used as a dopant in an emissive layer of the OLED, triplet exciton energy is transferred with exchanging electrons among adjacently disposed molecules in Dexter energy transfer mechanism. Owing to the reduced overlapping regions among the adjacent molecules, Dexter energy transfer mechanism in which triplet exciton energy of the host and other luminous materials is transferred to the triplet state of the organic compound is limited in case of using the organic compound as the ultimate luminous material. On the contrary, singlet exciton energy, not the triplet exciton energy, of the host and other luminous materials is likely to be transferred to the singlet state of the organic compound via FRET mechanism.

The organic compound having the structure of Chemical Formula 1 cannot utilize the triplet exciton energy because it is fluorescent material. The triplet exciton energy transferred to the organic compound via Dexter energy transfer mechanism cannot contribute to the luminescence of the organic compound. On the other hand, the singlet exciton energy transferred to the organic compound can participate in the luminescence process of the organic compound. As the Dexter energy transfer mechanism in which triplet exciton energy not contributing to the luminescence of the organic compound having the structure of Chemical Formula 1 is limited and singlet exciton energy is transferred to the organic compound via FRET mechanism which transfers only singlet-singlet exciton energy, the amount of exciton energies that can be utilized by the organic compound for luminescence is increased. When the organic compound is used as the ultimate luminous material, i.e. dopant in the EML, the OLED can its luminous efficiency and luminous lifetime. In addition, the organic compound includes the BODIPY moiety having narrow FWHM (Full-width at half maximum), thus it has excellent color purity. Moreover, it is possible to adjust luminescent colors by modifying the groups substituted to the BODIPY moiety. Therefore, it is possible to realize an OLED as well as an organic light emitting device which lowers its driving voltage, improves its luminous efficiency and color purity by applying the organic compound.

As an example, each of the C₁-Cao alkyl group, the C₁-Cao alkoxy group, the C₁-C₂₀ alkyl amino group, the C₆-C₃₀ aromatic group and the C₃-C₃₀ hetero aromatic group in R₁ to R₈ may independently unsubstituted or substituted with a C₁-C₂₀ alkyl group, a C₆-C₃₀ aryl group and a C₃-C₃₀ hetero aryl group and combination thereof.

In one exemplary aspect, at least four of R₁ to R₆ in Chemical Formula 1 is independently selected from the group consisting of an unsubstituted or substituted C₆-C₃₀ aryl group and an unsubstituted or substituted C₃-C₃₀ hetero aryl group. In this case, each of the C₆-C₃₀ aryl group and the C₃-C₃₀ hetero aryl group in R₁ to R₆ may be independently unsubstituted or substituted with a C₁-C₁₀ alkyl group. Also, any one of A₁ to A₄ constituting the fused aromatic ring is nitrogen, and at least one carbon atom adjacently to the nitrogen atom may be unsubstituted or substituted with a C₁-C₂₀ alkyl group, a C₁-C₂₀ alkyl amino group, a C₆-C₃₀ aryl group unsubstituted or substituted with a C₁-C₁₀ alkyl group and/or a C₃-C₃₀ hetero aryl group unsubstituted or substituted with a C₁-C₁₀ alkyl group.

In one exemplary aspect, the organic compound having the structure of Chemical Formula 1 may emit red light. The organic compound emitting red light may have a maximum photoluminescence peak (PL PL λ_(max)) between more than about 560 nm and about 670 nm, preferably between more than about 580 nm and about 650 nm, and may have a maximum absorption peak (Abs. λ_(max)) between more than about 550 nm and about 650 nm, preferably between more than about 560 nm and about 630 nm. As an example, the organic compound emitting red light may comprise an organic compound in which four groups in R₁ to R₆, for example, each of R₁, R₃, R₄ and R₆ is independently a C₆-C₃₀ aryl group unsubstituted or substituted with a C₁-C₁₀ alkyl group or a C₃-C₃₀ hetero aryl group unsubstituted or substituted with a C₁-C₁₀ alkyl group, respectively. Such an organic compound may comprise anyone having the following structure of Chemical Formula 2:

Alternatively, the organic compound emitting red light may comprise an organic compound in which at least five groups of R₁ to R₆ in Chemical Formula 1 is independently a C₆-C₃₀ aryl group unsubstituted or substituted with a C₁-C₁₀ alkyl group or a C₃-C₃₀ hetero aryl group unsubstituted or substituted with a C₁-C₁₀ alkyl group, respectively. Such an organic compound may comprise anyone having the following structure of Chemical Formula 3:

In another exemplary aspect, the organic compound having the structure of Chemical Formula 1 may emit green light. The organic compound emitting green light may have a maximum photoluminescence peak (PL PL λ_(max)) between more than about 500 nm and about 560 nm, preferably between more than about 510 nm and about 550 nm, and may have a maximum absorption peak (Abs. λ_(max)) between more than about 490 nm and about 550 nm, preferably between more than about 500 nm and about 550 nm. As an example, the organic compound emitting green light may comprise an organic compound in which four groups in R₁ to R₆, for example, each of R₁, R₃, R₄ and R₆ is independently hydrogen or a C₁-C₁₀ alkyl group, preferably a C₁-C₅ alkyl group. Such an organic compound may comprise anyone having the following structure of Chemical Formula 4:

Alternatively, the organic compound emitting green light may comprise an organic compound in which at least five groups of R₁ to R₆ in Chemical Formula 1 is independently a C₁-C₁₀ alkyl group, preferably a C₁-C₅ alkyl group, respectively. Such an organic compound may comprise anyone having the following structure of Chemical Formula 5:

[Organic Light Emitting Device and OLED]

The organic compound having the structure of Chemical Formulae 1 to 5 may be applied into an EML of the OLED, so that it can lower the driving voltage, enhance the color purity and improve the luminous efficiency of the OLED. The OLED of the present disclosure may be applied to an organic light emitting device such as an organic light emitting display device or an organic light emitting illumination device. An organic light emitting display device including the OLED will be explained. FIG. 1 is a schematic cross-sectional view of an organic light emitting display device in accordance with an aspect of the present disclosure. All components of the organic light emitting display device in accordance with all aspects of the present disclosure are operatively coupled and configured.

As illustrated in FIG. 1, the organic light emitting display device 100 includes a substrate 110, a thin-film transistor Tr on the substrate 110, and an organic light emitting diode (OLED) D connected to the thin film transistor Tr.

The substrate 110 may include, but is not limited to, glass, thin flexible material and/or polymer plastics. For example, the flexible material may be selected from the group, but is not limited to, polyimide (PI), polyethersulfone (PES), polyethylenenaphthalate (PEN), polyethylene terephthalate (PET), polycarbonate (PC) and combination thereof. The substrate 110, over which the thin film transistor Tr and the OLED D are arranged, form an array substrate.

A buffer layer 122 may be disposed over the substrate 110, and the thin film transistor Tr is disposed over the buffer layer 122. The buffer layer 122 may be omitted.

A semiconductor layer 120 is disposed over the buffer layer 122. In one exemplary aspect, the semiconductor layer 120 may include, but is not limited to, oxide semiconductor materials. In this case, a light-shield pattern may be disposed under the semiconductor layer 120, and the light-shield pattern can prevent light from being incident toward the semiconductor layer 120, and thereby, preventing the semiconductor layer 120 from being deteriorated by the light. Alternatively, the semiconductor layer 120 may include, but is not limited to, polycrystalline silicon. In this case, opposite edges of the semiconductor layer 120 may be doped with impurities.

A gate insulating layer 124 formed of an insulating material is disposed on the semiconductor layer 120. The gate insulating layer 124 may include, but is not limited to, an inorganic insulating material such as silicon oxide (SiO_(x)) or silicon nitride (SiN_(x)).

A gate electrode 130 made of a conductive material such as a metal is disposed over the gate insulating layer 124 so as to correspond to a center of the semiconductor layer 120. While the gate insulating layer 124 is disposed over a whole area of the substrate 110 in FIG. 1, the gate insulating layer 124 may be patterned identically as the gate electrode 130.

An interlayer insulating layer 132 formed of an insulating material is disposed on the gate electrode 130 with covering over an entire surface of the substrate 110. The interlayer insulating layer 132 may include, but is not limited to, an inorganic insulating material such as silicon oxide (SiO_(x)) or silicon nitride (SiN_(x)), or an organic insulating material such as benzocyclobutene or photo-acryl.

The interlayer insulating layer 132 has first and second semiconductor layer contact holes 134 and 136 that expose both sides of the semiconductor layer 120. The first and second semiconductor layer contact holes 134 and 136 are disposed over opposite sides of the gate electrode 130 with spacing apart from the gate electrode 130. The first and second semiconductor layer contact holes 134 and 136 are formed within the gate insulating layer 124 in FIG. 1. Alternatively, the first and second semiconductor layer contact holes 134 and 136 are formed only within the interlayer insulating layer 132 when the gate insulating layer 124 is patterned identically as the gate electrode 130.

A source electrode 144 and a drain electrode 146, which are formed of conductive material such as a metal, are disposed on the interlayer insulating layer 132. The source electrode 144 and the drain electrode 146 are spaced apart from each other with respect to the gate electrode 130, and contact both sides of the semiconductor layer 120 through the first and second semiconductor layer contact holes 134 and 136, respectively.

The semiconductor layer 120, the gate electrode 130, the source electrode 144 and the drain electrode 146 constitute the thin film transistor Tr, which acts as a driving element. The thin film transistor Tr in FIG. 1 has a coplanar structure in which the gate electrode 130, the source electrode 144 and the drain electrode 146 are disposed over the semiconductor layer 120. Alternatively, the thin film transistor Tr may have an inverted staggered structure in which a gate electrode is disposed under a semiconductor layer and a source and drain electrodes are disposed over the semiconductor layer. In this case, the semiconductor layer may comprise amorphous silicon.

A gate line and a data line, which cross each other to define a pixel region, and a switching element, which is connected to the gate line and the data line, may be further formed in the pixel region of FIG. 1. The switching element is connected to the thin film transistor Tr, which is a driving element. Besides, a power line is spaced apart in parallel from the gate line or the data line, and the thin film transistor Tr may further include a storage capacitor configured to constantly keep a voltage of the gate electrode for one frame.

In addition, the organic light emitting display device 100 may include a color filter that comprises dyes or pigments for transmitting specific wavelength light of light emitted from the OLED D. For example, the color filter can transmit light of specific wavelength such as red (R), green (G) and/or blue (B). Each of red, green, and blue color filter may be formed separately in each pixel region. In this case, the organic light emitting display device 100 can implement full-color through the color filter.

For example, when the organic light emitting display device 100 is a bottom-emission type, the color filter may be disposed on the interlayer insulating layer 132 with corresponding to the OLED D. Alternatively, when the organic light emitting display device 100 is a top-emission type, the color filter may be disposed over the OLED D, that is, a second electrode 230.

A passivation layer 150 is disposed on the source and drain electrodes 144 and 146 over the whole substrate 110. The passivation layer 150 has a flat top surface and a drain contact hole 152 that exposes the drain electrode 146 of the thin film transistor Tr. While the drain contact hole 152 is disposed on the second semiconductor layer contact hole 136, it may be spaced apart from the second semiconductor layer contact hole 136.

The OLED D includes a first electrode 210 that is disposed on the passivation layer 150 and connected to the drain electrode 146 of the thin film transistor Tr. The OLED D further includes an emissive layer 220 and a second electrode 230 each of which is disposed sequentially on the first electrode 210.

The first electrode 210 is disposed in each pixel region. The first electrode 210 may be an anode and include a conductive material having a relatively high work function value. For example, the first electrode 210 may include, but is not limited to, a transparent conductive material such as indium tin oxide (ITO), indium zinc oxide (IZO), indium tin zinc oxide (ITZO), tin oxide (SnO), zinc oxide (ZnO), indium cerium oxide (ICO), aluminum doped zinc oxide (AZO), and the like.

In one exemplary aspect, when the organic light emitting display device 100 is a top-emission type, a reflective electrode or a reflective layer may be disposed under the first electrode 210. For example, the reflective electrode or the reflective layer may include, but are not limited to, aluminum-palladium-copper (APC) alloy.

In addition, a bank layer 160 is disposed on the passivation layer 150 in order to cover edges of the first electrode 210. The bank layer 160 exposes a center of the first electrode 210.

An emissive layer 220 is disposed on the first electrode 210. In one exemplary aspect, the emissive layer 220 may have a mono-layered structure of an emitting material layer (EML). Alternatively, the emissive layer 220 may have a multiple-layered structure of a hole injection layer (HIL), a hole transport layer (HTL), an electron blocking layer (EBL), an EML, a hole blocking layer (HBL), an electron transport layer (ETL) and/or an electron injection layer (EIL) (see, FIGS. 2, 4, 7 and 9). In one aspect, the emissive layer 220 may have one emitting unit. Alternatively, the emissive layer 220 may have multiple emitting units to form a tandem structure.

The emissive layer 220 comprises anyone having the structure of Chemical Formulae 1 to 5. As an example, the organic compound having the structure of Chemical Formulae 1 to 5 may be applied into a dopant in the EML, and in this case, the EML may further comprise a host and optionally other luminous materials.

The second electrode 230 is disposed over the substrate 110 above which the emissive layer 220 is disposed. The second electrode 230 may be disposed over a whole display area and may include a conductive material with a relatively low work function value compared to the first electrode 210. The second electrode 230 may be a cathode. For example, the second electrode 230 may include, but is not limited to, aluminum (Al), magnesium (Mg), calcium (Ca), silver (Ag), alloy thereof or combination thereof such as aluminum-magnesium alloy (Al—Mg).

In addition, an encapsulation film 170 may be disposed over the second electrode 230 in order to prevent outer moisture from penetrating into the OLED D. The encapsulation film 170 may have, but is not limited to, a laminated structure of a first inorganic insulating film 172, an organic insulating film 174 and a second inorganic insulating film 176.

Moreover, a polarizer may be attached to the encapsulation film 170 in order to decrease external light reflection. For example, the polarizer may be a circular polarizer. In addition, a cover window may be attached to the encapsulation film 170 or the polarizer. In this case, the substrate 110 and the cover window may have a flexible property, thus the organic light emitting display device 100 may be a flexible display device.

Now, we will describe the OLED in more detail. FIG. 2 is a schematic cross-sectional view illustrating an OLED in accordance with an exemplary aspect of the present disclosure. As illustrated in FIG. 2, the OLED D1 includes first and second electrodes 210 and 230 facing each other and an emissive layer 220 having single emitting unit disposed between the first and second electrodes 210 and 230. In one exemplary aspect, the emissive layer 220 comprises an EML 240 disposed between the first and second electrodes 210 and 230. Also, the emissive layer 220 further comprises a HIL 250 and a HTL 260 each of which is disposed sequentially between the first electrode 210 and the EML 240, and an ETL 270 and an EIL 280 each of which is disposed sequentially between the EML 240 and the second electrode 230. Alternatively, the emissive layer 220 may further comprise a first exciton blocking layer, i.e. an EBL 265 disposed between the HTL 260 and the EML 240 and/or a second exciton blocking layer, i.e. a HBL 275 disposed between the EML 240 and the ETL 270.

The first electrode 210 may be an anode that provides a hole into the EML 240. The first electrode 210 may include, but is not limited to, a conductive material having a relatively high work function value, for example, a transparent conductive oxide (TCO). In an exemplary aspect, the first electrode 210 may include, but is not limited to, ITO, IZO, ITZO, SnO, ZnO, ICO, AZO, and the like.

The second electrode 230 may be a cathode that provides an electron into the EML 240. The second electrode 230 may include, but is not limited to, a conductive material having a relatively low work function values, i.e., a highly reflective material such as Al, Mg, Ca, Ag, alloy thereof, combination thereof, and the like.

The HIL 250 is disposed between the first electrode 210 and the HTL 260 and improves an interface property between the inorganic first electrode 210 and the organic HTL 260. In one exemplary aspect, the HIL 250 may include, but is not limited to, 4,4′4″-Tris(3-methylphenylamino)triphenylamine (MTDATA), 4,4′,4″-Tris(N,N-diphenyl-amino)triphenylamine (NATA), 4,4′,4″-Tris(N-(naphthalene-1-yl)-N-phenyl-amino)triphenylamine (1T-NATA), 4,4′,4″-Tris(N-(naphthalene-2-yl)-N-phenyl-amino)triphenylamine (2T-NATA), Copper phthalocyanine (CuPc), Tris(4-carbazoyl-9-yl-phenyl)amine (TCTA), N,N′-Diphenyl-N,N′-bis(1-naphthyl)-1,1′-biphenyl-4,4″-diamine (NPB; NPD), 1,4,5,8,9,11-Hexaazatriphenylenehexacarbonitrile (Dipyrazino[2,3-f: 2′3′-h]quinoxaline-2,3,6,7,10,11-hexacarbonitrile; HAT-CN), 1,3,5-tris[4-(diphenylamino)phenyl]benzene (TDAPB), poly(3,4-ethylenedioxythiphene)polystyrene sulfonate (PEDOT/PSS) and/or N-(biphenyl-4-yl)-9,9-dimethyl-N-(4-(9-phenyl-9H-carbazol-3-yl)phenyl)-9H-fluoren-2-amine. The HIL 250 may be omitted in compliance with a structure of the OLED D1.

The HTL 260 is disposed adjacently to the EML 240 between the first electrode 210 and the EML 240. In one exemplary aspect, the HTL 260 may include, but is not limited to, N,N′-Diphenyl-N,N′-bis(3-methylphenyl)-1,1′-biphenyl-4,4′-diamine (TPD), NPB, 4,4′-bis(N-carbazolyl)-1,1′-biphenyl (CBP), Poly[N,N′-bis(4-butylphenyl)-N,N′-bis(phenyl)-benzidine] (Poly-TPD), Poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-(4,4′-(N-(4-sec-butylphenyl)diphenylamine))] (TFB), Di-[4-(N,N-di-p-tolyl-amino)-phenyl] cyclohexane (TAPC), N-(biphenyl-4-yl)-9,9-dimethyl-N-(4-(9-phenyl-9H-carbazol-3-yl)phenyl)-9H-fluoren-2-amine and/or N-(biphenyl-4-yl)-N-(4-(9-phenyl-9H-carbazol-3-yl)phenyl)biphenyl-4-amine.

In the first aspect, the EML 240 may comprise a first compound (Compound 1, Host) H and a second compound (Compound 2) FD. For example, the first compound H may be a (first) host and the second compound FD may be a fluorescent material (first dopant). As an example, the organic compound having the structure of Chemical Formulae 1 to 5 may be used the second compound FD. In this case the EML 240 may emit red or green light.

When the EML 240 comprises the first compound H that may the host and the second compound FD which may be anyone having the structure of Chemical Formulae 1-5, it may be necessary to adjust excited singlet and triplet energy levels among the luminous materials. FIG. 3 is a schematic diagram illustrating luminous mechanism by energy level bandgap among luminous materials in accordance with this exemplary aspect of the present disclosure.

As illustrated in FIG. 3, an excited singlet energy level S₁ ^(H) of the first compound H, which may be the host, is higher than an excited singlet energy level S₁ ^(FD) of the second compound FD, which may be the fluorescent material. Alternatively, an excited triplet energy level T₁ ^(H) of the first compound H may be higher than an excited triplet energy level T₁ ^(FD) of the second compound FD. In this case, the exciton energy generated at the first compound H may be transferred to the second compound FD. The first compound H may have a PL spectrum overlapping widely to an Abs. spectrum of the second compound FD, thus the exciton energy can be efficiently transferred from the first compound H to the second compound FD. As an example, the first compound H may have a maximum absorption peak (Abs. λ_(max)), but is not limited to, between about 500 nm and about 600 nm.

In one exemplary aspect, the first compound H that can be used as the host in the EML 240 may comprise, but is not limited to, 9,9′-Diphenyl-9H,9′H-3,3′-bicarbazole (BCzPh), 1,3,5-Tris(carbazole-9-yl)benzene (TCP), TCTA, CBP, 4,4′-Bis(carbazole-9-yl)-2,2′-dimethylbipheyl (CDBP), 2,7-Bis(carbazole-9-yl)-9,9-dimethylfluorene (DMFL-CBP), 2,2′,7,7′-Tetrakis(carbazole-9-yl)-9,9-spiorofluorene (spiro-CBP), Bis[2-(diphenylphosphino)phenyl] ether oxide (DPEPO), 4′-(9H-carbazol-9-yl)biphenyl-3,5-dicarbonitrile (PCzB-2CN), 3′-(9H-carbazol-9-yl)biphenyl-3,5-dicarbonitrile (mCzB-2CN), 3,6-Bis(carbazole-9-yl)-9-(2-ethyl-hexyl)-9H-carbazole (TCz1), 9-(3-(9H-carbazol-9-yl)phenyl)-9H-carbazole-3-carbonitrile (mCP-CN), 3,3′-bis(N-carbazolyl)-1,1′-biphenyl (mCBP), 1,3-Bis(carbazol-9-yl)benzene (mCP), 2,8-bis(diphenylphosphoryl)dibenzothiophene (PPT), 1,3,5-Tri[(3-pyridyl)-phen-3-yl]benzene (TmPyPB), 2,6-Di(9H-carbazol-9-yl)pyridine (PYD-2Cz), Bis(2-hydroxylphenyl)-pyridine)beryllium (Bepp2), Bis(10-hydroxylbenzo[h] quinolinato)beryllium (Bebq2), 1,3,5-Tris(1-pyrenyl)benzene (TPB3), 2,8-di(9H-carbazol-9-yl)dibenzothiophene (DCzDBT), 3′,5′-Di(carbazol-9-yl)-[1,1-bipheyl]-3,5-dicarbonitrile (DCzTPA), Diphenyl-4-triphenylsilylphenyl-phosphine oxide (TSPO1), 9-(9-phenyl-9H-carbazol-6-yl)-9H-carbazole (CCP), 4-(3-(triphenylen-2-yl)phenyl)dibenzo[b,d]thiophene, 9-(4-(9H-carbazol-9-yl)phenyl)-9H-3,9′-bicarbazole, 9-(3-(9H-carbazol-9-yl)phenyl)-9H-3,9′-bicarbazole) and/or 9-(6-(9H-carbazol-9-yl)pyridin-3-yl)-9H-3,9′-bicabazole.

When the EML 240 comprise the first compound H and the second compound FD, the contents of the second compound FD may be, but is not limited to, about 1 wt % to about 50 wt %, preferably about 1 wt % to about 30 wt %.

The ETL 270 and the EIL 280 may be disposed sequentially between the EML 240 and the second electrode 230. The ETL 270 includes a material having high electron mobility so as to provide electrons stably with the EML 240 by fast electron transportation.

In one exemplary aspect, the ETL 270 may comprise, but is not limited to, oxadiazole-based compounds, triazole-based compounds, phenanthroline-based compounds, benzoxazole-based compounds, benzothiazole-based compounds, benzimidazole-based compounds, triazine-based compounds, and the like.

As an example, the ETL 270 may comprise, but is not limited to, tris-(8-hydroxyquinoline aluminum (Alq₃), 2-biphenyl-4-yl-5-(4-t-butylphenyl)-1,3,4-oxadiazole (PBD), spiro-PBD, lithium quinolate (Liq), 1,3,5-Tris(N-phenylbenzimidazol-2-yl)benzene (TPBi), Bis(2-methyl-8-quinolinolato-N1,08)-(1,1′-biphenyl-4-olato)aluminum (BAlq), 4,7-diphenyl-1,10-phenanthroline (Bphen), 2,9-Bis(naphthalene-2-yl)4,7-diphenyl-1,10-phenanthroline (NBphen), 2,9-Dimethyl-4,7-diphenyl-1,10-phenaathroline (BCP), 3-(4-Biphenyl)-4-phenyl-5-tert-butylphenyl-1,2,4-triazole (TAZ), 4-(Naphthalen-1-yl)-3,5-diphenyl-4H-1,2,4-triazole (NTAZ), 1,3,5-Tri(p-pyrid-3-yl-phenyl)benzene (TpPyPB), 2,4,6-Tris(3′-(pyridin-3-yl)biphenyl-3-yl)1,3,5-triazine (TmPPPyTz), Poly[9,9-bis(3′-(N,N-dimethyl)-N-ethylammonium)-propyl)-2,7-fluorene]-alt-2,7-(9,9-dioctylfluorene)] (PFNBr), tris(phenylquinoxaline) (TPQ) and/or TSPO1.

The EIL 280 is disposed between the second electrode 230 and the ETL 270, and can improve physical properties of the second electrode 230 and therefore, can enhance the lifetime of the OLED D1. In one exemplary aspect, the EIL 280 may comprise, but is not limited to, an alkali halide such as LiF, CsF, NaF, BaF₂ and the like, and/or an organic metal compound such as lithium quinolate, lithium benzoate, sodium stearate, and the like.

When holes are transferred to the second electrode 230 via the EML 240 and/or electrons are transferred to the first electrode 210 via the EML 240, the OLED D1 may have short lifetime and reduced luminous efficiency. In order to prevent these phenomena, the OLED D1 in accordance with this aspect of the present disclosure may have at least one exciton blocking layer adjacent to the EML 240.

For example, the OLED D1 of the exemplary aspect includes the EBL 265 between the HTL 260 and the EML 240 so as to control and prevent electron transfers. In one exemplary aspect, the EBL 265 may comprise, but is not limited to, TCTA, Tris[4-(diethylamino)phenyl]amine, N-(biphenyl-4-yl)-9,9-dimethyl-N-(4-(9-phenyl-9H-carbazol-3-yl)phenyl)-9H-fluorene-2-amine, TAPC, MTDATA, mCP, mCBP, CuPc, N,N′-bis[4-(bis(3-methylphenyl)amino)phenyl]-N,N′-diphenyl-[1,1′-biphenyl]-4,4′-diamine (DNTPD), TDAPB, 3,5-di(9H-carbazol-9-yl)-N,N-diphenylamine (DCDPA) and/or 3,6-bis(N-carbazolyl)-N-phenyl-carbazole.

In addition, the OLED D1 may further include the HBL 275 as a second exciton blocking layer between the EML 240 and the ETL 270 so that holes cannot be transferred from the EML 240 to the ETL 270. In one exemplary aspect, the HBL 275 may comprise, but is not limited to, oxadiazole-based compounds, triazole-based compounds, phenanthroline-based compounds, benzoxazole-based compounds, benzothiazole-based compounds, benzimidazole-based compounds, and triazine-based compounds each of which can be used in the ETL 270.

For example, the HBL 275 may comprise a compound having a relatively low HOMO energy level compared to the luminescent materials in EML 240. The HBL 275 may comprise, but is not limited to, mCBP, BCP, BAlq, Alq₃, PBD, spiro-PBD, Liq, Bis-4,5-(3,5-di-3-pyridylphenyl)-2-methylpyrimidine (B3PYMPM), DPEPO, 9-(6-(9H-carbazol-9-yl)pyridine-3-yl)-9H-3,9′-bicarbazole and combination thereof.

In accordance with this aspect, the EML 240 comprises the first compound H and the second compound FD that is any organic compound having the structure of Chemical Formulae 1 to 5. The organic compound has a less spike-like structure compared to the conventional red or green fluorescent materials, thus there exist less overlapping regions among the adjacent molecules and distance among the adjacent molecules increases. Accordingly, since the triplet energy transfer by Dexter energy transfer mechanism is limited, but the singlet exciton energy is mainly transferred from the first compound to the second compound via FRET mechanism. In other words, as Dexter transfer energy mechanism which triplet exciton energy transfers as a non-radiative recombination is minimized, it is likely that the singlet exciton energy contributing emission is transferred to the second compound. Accordingly, the OLED D2 which applies the organic compound into the EML 240 can be driven at low voltage and improve its luminous efficiency and color purity.

In the above aspect, the EML consists of the first compound that may be the host and the second compound that may the fluorescent material or dopant. Unlike that aspect, the EML may comprise plural dopants having different luminous properties. FIG. 4 is a schematic cross-sectional view illustrating an OLED in accordance with another exemplary aspect of the present disclosure. As illustrated in FIG. 4, the OLED D2 comprises the first electrode 210, the second electrode 230 facing the first electrode 210 and an emissive layer 220A disposed between the first and second electrodes 210 and 230. The emissive layer 220A having single emitting unit comprises an EML 240A. Also, the emissive layer 220A comprise the HIL 250 and the HTL 260 each of which is disposed sequentially between the first electrode 210 and the EML 240A, and the ETL 270 and the EIL 280 each of which is disposed sequentially between the EML 240A and the second electrode 230. Alternatively, the emissive layer 220A may further comprise the EBL 265 disposed between the HTL 260 and the EML 240A and/or the HBL 275 disposed between the EML 240A and the ETL 270. The configurations of the first and second electrodes 210 and 230 as well as other layers except the EML 240A in the emissive layer 220A may be substantially identical to the corresponding electrodes and layers in the OLED D1.

In this aspect, the EML 240A comprise the first compound (Compound 1, Host) H, the second compound (Compound 2) FD and a third compound (Compound 3) DF. The first compound H may be the host, the second compound FD may be the fluorescent material (second dopant) and the third compound DF may be delayed fluorescent material (first dopant). The second compound FD may comprise any organic compound having the structure of Chemical Formulae 1 to 5. When the EML 240A comprises the delayed fluorescent material, it is possible to realize OLED D2 having much enhanced luminous efficiency by adjusting energy levels among the host and the dopants.

An external quantum efficiency (EQE, η_(ext)) of the luminous material in an EML can be calculated as the following Equation:

η_(ext)=η_(S/T)×Γ×Φ×η_(out-coupling)

-   -   wherein η_(S/T) is a singlet/triplet ratio; Γ is a charge         balance factor; Φ is a radiative efficiency; and         η_(out-coupling) is an out-coupling efficiency.

When holes and electrons meet to form exciton, singlet exciton with a paired spin state and triplet exciton with an unpaired spin state is generated in a ratio of 1:3 in theory. Since only the singlet exciton participates in luminescence and the remaining 75% triplet excitons cannot participate in luminescence in the fluorescent material, the singlet/triplet ratio is 0.25 in the conventional fluorescent material.

The charge balance factor Γ indicates a balance of holes and electrons forming excitons and generally has “1” assuming 100% 1:1 matching. The radiative efficiency Φ is a value involved in luminous efficiency of the substantial luminous materials and depends upon the photoluminescence of the dopant in the host-dopant system. The out-coupling efficiency is a ratio of extracted externally light among the emitted light form the luminous material. When a thin film is used by depositing the luminous material with isotropic type, each luminous molecule is existed randomly without any specific orientation. The out-coupling efficiency in such random orientation is assumed “0.2”. Therefore, when taking all four factors defined in the above Equation into account, the maximum luminous efficiency of the OLED using the conventional fluorescent material is only about 5%.

On the other hand, phosphorescent materials have a luminescent mechanism that converts both the singlet and triplet excitons to light. Phosphorescent materials convert singlet exciton into triplet exciton through intersystem crossing (ISC). Therefore, when using phosphorescent materials using both singlet exciton and triplet exciton, it is possible to improve the low luminous efficiency of the fluorescent materials. However, blue phosphorescent materials have too low color purity and too short lifetime to be applied into commercial display devices. Thus, it is necessary to improve the disadvantages of the phosphorescent materials and the low luminous efficiency of the blue luminescent materials.

Recently, a delayed fluorescent material, which can solve the problems accompanied by the conventional art fluorescent and/or phosphorescent materials, has been developed. Representative delayed fluorescent material is a thermally-activated delayed fluorescent (TADF) material. Since the delayed fluorescent material generally has both an electron donor moiety and an electron acceptor moiety within its molecular structure, it can be converted to an intramolecular charge transfer (ICT) state. In case of using the delayed fluorescent material as a dopant, it is possible to use both the singlet energy and the triplet energy during the luminescent process, unlike the conventional fluorescent materials.

The luminous mechanism of the delayed fluorescent material will be explained with referring to FIG. 5, which is a schematic diagram illustrating a luminous mechanism of delayed fluorescent material in the EML. As illustrated in FIG. 5, the excitons of singlet energy level S₁ ^(DF) as well as the excitons of triplet energy level T₁ ^(DF) in the delayed fluorescent material DF can be transferred to an intermediate energy level state, i.e. ICT state, and then the intermediate stated excitons can be shifted to a ground state (S₀ ^(DF); S₁ ^(DF)→ICT←T₁ ^(DF)). Since the excitons of singlet energy level S₁ ^(DF) as well as the excitons of triplet energy level T₁ ^(DF) in the delayed fluorescent material DF is involved in the luminescent process, the delayed fluorescent material DF can improve its luminous efficiency.

Since both the HOMO and the LUMO are widely distributed over the whole molecule within the common fluorescent material, it is not possible to inter-convert exciton energies between the singlet energy level and the triplet energy level within the common fluorescent material (selection rule). In contrast, since the delayed fluorescent material DF, which can be converted to ICT state, has little orbital overlaps between HOMO and LUMO, there is little interaction between the HOMO state and the LUMO state. As a result, the changes of spin states of electrons do not have an influence on other electrons, and a new charge transfer band (CT band) that does not follow the selection rule is formed within the delayed fluorescent material.

In other words, since the delayed fluorescent material DF has the electron acceptor moiety spacing apart from the electron donor moiety within the molecule, it exists as a polarized state having a large dipole moment within the molecule. As the interaction between HOMO and LUMO becomes little in the state where the dipole moment is polarized, the triplet excitons as well as the singlet excitons can be converted to ICT state. In other words, ICT complex can be excited to a CT state in which singlet exciton and triplet exciton can be exchanged mutually, thus the triplet excitons as well as singlet excitons can be involved in the luminescent process. In case of driving an OLED that includes the delayed fluorescent material DF, both 25% singlet excitons and 75% triplet excitons are converted to ICT state by heat or electrical field, and then the converted excitons drops to the ground state S₀ with luminescence. Therefore, the delayed fluorescent material DF may have 100% internal quantum efficiency in theory.

The delayed fluorescent material DF must has an energy level bandgap ΔE_(ST) ^(DF) equal to or less than about 0.3 eV, for example, from about 0.05 to about 0.3 eV, between the excited singlet energy level S₁ ^(DF) and the excited triplet energy level T₁ ^(DF) so that exciton energy in both the excited singlet energy level S₁ ^(DF) and the excited triplet energy level T₁ ^(DF) can be transferred to the ICT state. The material having little energy level bandgap between the singlet energy level S₁ ^(DF) and the triplet energy level T₁ ^(DF) can exhibit common fluorescence with Inter system Crossing (ISC) in which the excitons of singlet energy level S₁ ^(DF) can be shifted to the ground state, as well as delayed fluorescence with Reverser Inter System Crossing (RISC) in which the excitons of triplet energy level T₁ ^(DF) can be transferred upwardly to the excitons of singlet energy level S₁ ^(DF), and then the exciton of singlet energy level S₁ ^(DF) transferred from the triplet energy level T₁ ^(DF) can be shifted to the ground state S₀ ^(DF).

As described above, the thermally-delayed fluorescent material should reduce the overlap between HOMO and LUMO and have electron acceptor spacing apart from electron donor so as to minimize the energy bandgap ΔE_(ST) ^(DF) between the excited singlet energy level S₁ ^(DF) and the excited triplet energy level T₁ ^(DF). Since the molecular conformation of the excited state and the ground state is twisted in the molecules having less overlaps between the HOMO and the LUMO and spaced apart electron donor-electron acceptor, the delayed fluorescent material has short luminous lifetime and addition charge transfer transition (CT transition) is caused in the delayed fluorescent material. Due to the luminous property caused by the CT luminous mechanism, the delayed fluorescent material has luminous wavelength with wide FWHM (full width at half maximum, and thus shows deteriorated color purity.

However, the triplet exciton of the delayed fluorescent material is converted to its own singlet exciton and then the converted singlet exciton of the delayed fluorescent material is transferred to the fluorescent material in hyper fluorescence, thus increases the singlet exciton generation ratio of the fluorescent materials which utilizes only the singlet exciton. As described above, since the delayed fluorescent material utilized both the singlet exciton energy and the triplet exciton energy, the fluorescent material absorbs the singlet and triplet exciton energies emitted from the delayed fluorescent material, and the fluorescent material generate 100% singlet exciton utilizing the absorbed exciton energies in luminescence process, so the luminous efficiency of the fluorescent material can be improved. As an example, as the ultimate light emission occurs at the fluorescent material, color purity can be enhanced in case of using the fluorescent material with relatively narrow FWHM. In addition, since the luminous lifetime is determined by the fluorescent material, the EML having both the delayed fluorescent material and the fluorescent material can improve its luminous lifetime and stability compared to the EML having only the delayed fluorescent material.

As described above, the EML 240A comprise the first compound H that may be the host, the second compound FD that may be the fluorescent material and may be anyone having the structure of Chemical Formulae 1 to 5, and the third compound DF that may be the delayed fluorescent material. In this case, it is necessary to adjust energy levels among the luminous materials in order to transfer exciton energy among the first to third compounds. FIG. 6 is a schematic diagram illustrating luminous mechanism by energy level bandgap among luminous materials in accordance with another exemplary aspect of the present disclosure.

As illustrated in FIG. 6, the exciton energy generated at the first compound H should be transferred primarily to the third compound DF that may the delayed fluorescent material. To this end, each of the excited singlet energy level S₁ ^(H) and the excited triplet energy level T₁ ^(H) of the first compound H, which can be the host in the EML 240, is higher than each of the excited singlet energy level SP and the excited triplet energy level of the third compound DF having the delayed fluorescent property, respectively.

For example, when the excited triplet energy level T₁ ^(H) of the first compound H is not high enough than the excited triplet energy level of the third compound DF, the triplet state exciton energy of the third compound DF may be reversely transferred to the excited triplet energy level T₁ ^(H) of the first compound H. In this case, the triplet exciton reversely transferred to the first compound H where the triplet exciton cannot be emitted is quenched as non-emission so that the triplet exciton energy of the third compound DF having the delayed fluorescent property cannot contribute to luminescence. As an example, the excited triplet energy level T₁ ^(H) of the first compound H may be higher than the excited triplet energy level T₁ ^(DF) of the third compound DF by at least about 0.5 eV, e.g. at least about 0.2 eV.

The third compound DF having the delayed fluorescent property may have the energy level bandgap ΔE_(ST) ^(DF) between the excited singlet energy level S₁ ^(DF) and the excited triplet energy level T₁ ^(DF) equal to or less than about 0.3 eV, for example between about 0.05 eV and about 0.3 eV (see, FIG. 5). On the contrary, each of the energy level bandgap between the excited singlet energy level S₁ ^(H) and the excited triplet energy level T₁ ^(H) of the first compound H, that may be the host, and the energy level bandgap between the excited singlet energy level S₁ ^(FD) and the excited triplet energy level T₁ ^(FD) of the second compound FD, that may be the fluorescent material, may be more than about 0.3 eV, respectively.

When the energy level bandgap between the singlet energy level and the triplet energy level of the first compound H and the second compound FD is more than about 0.3 eV, the OLED D2 may have short luminous lifetime owing to RISC mechanism and ISC mechanism caused by those compounds. For example, each of the energy level bandgap between the excited singlet energy level S₁ ^(H) and the excited triplet energy level T₁ ^(H) of the first compound H and the energy level bandgap between the excited singlet energy level S₁ ^(FD) and the excited triplet energy level T₁ ^(FD) of the second compound FD may be, but is not limited to, more than 0.3 eV and less than or equal to about 1.5 eV.

In addition, it is necessary to adjust properly HOMO energy levels and LUMO energy levels of the first compound H and the third compound DF. For example, it is preferable that an energy level bandgap (|HOMO^(H)-HOMO^(DF)|) between the HOMO energy level (HOMO^(H)) of the first compound H and the HOMO energy level (HOMO^(DF)) of the third compound DF, or an energy level bandgap (|LUMO^(H)-LUMO^(DF)|) between the LUMO energy level (LUMO^(H)) of the first compound H and the LUMO energy level (LUMO^(DF)) of the third compound DF may be equal to or less than about 0.5 eV, for example, between about 0.1 eV to about 0.5 eV. In this case, the charges can be transported efficiently from the first compound H as the host to the third compound DF as the delayed fluorescent material and thereby enhancing the ultimate luminous efficiency in the EML 240A.

In addition, it is necessary for the EML 240A to implement high luminous efficiency and color purity as well as to transfer exciton energy efficiently from the third compound DF, which is converted to ICT complex state by RISC mechanism in the EML 240A, to the second compound FD which is the fluorescent material in the EML 240A. To this end, the excited triplet energy level T₁ ^(DF) of the third compound DF is higher than the excited triplet energy level T₁ ^(FD) of the second compound FD. Optionally, the excited singlet energy level S₁ ^(DF) of the third compound DF may be higher than the excited singlet energy level S₁ ^(DF) of the second compound FD.

The exciton energy can be transferred from the third compound DF of the delayed fluorescent material to the second compound FD of the fluorescent material via FRET mechanism and Dexter mechanism. In FRET mechanism, singlet exciton energy is transferred as non-radiative though an electrical field caused by dipole-dipole interaction. On the other hand, in Dexter mechanism, exciton energy is transferred between triplet-triplet excitons or single-singlet exciton in which the delayed fluorescent material as an energy donor and the fluorescent material as an energy acceptor exchange directly their electrons.

As described above, the organic compound having the structure of Chemical Formulae 1 to 5 has little plate-like structures, and there exist less overlapping regions among adjacent molecules as the distance among them increases. When the second compound FD that may be any organic compound having the structure of Chemical Formulae 1 to 5 is introduced in the EML 240A, the triplet exciton energy transfer between the third compound DF of the delayed fluorescent material and the second compound FD through Dexter energy transfer mechanism is minimized, while the singlet exciton energy of the third compound DD is mainly transferred to the second compound FD through FRET mechanism. The triplet exciton energy, which cannot be utilized by the second compound FD, is little transferred to the second compound FD through Dexter mechanism, but the singlet exciton energy, which can be utilized by the second compound FD, is mainly transferred to the second compound FD by FRET mechanism. Accordingly, triplet exciton energy loss as a non-radiative recombination can be minimized. Therefore, the OLED D2 including the second compound FD of any organic compound having the structure of Chemical Formulae 1 to 5 can lower its driving voltage and improve its luminous efficiency and color purity to implement hyper fluorescence.

According to this aspect, the EML 240A comprises any organic compound having the structure of Chemical Formulae 1 to 5 as the fluorescent material in order to prevent the color purity from being deteriorated when an EML comprises the third compound DF having the delayed fluorescent property. The triplet exciton energy of the third compound DF is converted upwardly to its own singlet exciton energy by RISC, the converted singlet exciton energy of the third compound DF is transferred to the second compound FD having fluorescent property in the same layer via FRET mechanism, and thus exciton energy loss can be minimized.

In the hyper fluorescence mechanism comprising the ultimately emitted fluorescent material, it is important to transfer exciton energy from the delayed fluorescent material to the fluorescent material in order to improve its luminous efficiency. The most important factor determining the exciton energy transfer efficiency between the delayed fluorescent material and the fluorescent material is overlapping area between the PL spectrum of the delayed fluorescent material and the Abs. spectrum of the fluorescent material receiving the exciton energy. As the overlapping area between the PL spectrum of the third compound DF of the delayed fluorescent material and the Abs. spectrum of the second compound FD of the fluorescent material increases, the OLED D can improve its luminous efficiency. In addition, luminescence is occurred as the second compound FD of the fluorescent material shifts from the excited state to the ground state, not the third compound DF caused by CT mechanism, the OLED D can improve its color purity.

In one exemplar aspect, the second compound FD may emit red light. In this case, the second compound FD may have PL λ_(max) between more than about 560 nm and about 670 nm, preferably between more than about 580 nm and about 650 nm, may have Abs. λ_(max) between more than about 550 nm and about 650 nm, preferably between more than about 560 nm and about 630 nm, and may have the structure of Chemical Formula 2 or 3. In this case, the third compound DF of the delayed fluorescent material may have PL λ_(max) between about more than 500 nm and about 650 nm, preferably between about more than 550 nm and about 630 nm.

As an example, when the second compound FD emits red light, the third compound DF appropriate for transferring exciton energy to the second compound FD may comprise, but is not limited to, a benzonitrile-based compound having a cyano moiety as an electron acceptor moiety, a triazine-based compound having a phenoxazine moiety, an aromatic or hetero aromatic amino moiety and derivative thereof as an electron donor moiety and a triazine moiety and derivative thereof as an electron acceptor moiety and/or a quinoxaline-based compound.

For example, the third compound DF that can be used with the second compound FD emitting red light may comprise, but is not limited to, 6,11-di(10H-phenoxazin-10-yl)dibenzo[f,h]quinoxaline (ATP-PXZ), 7,10-di(10H-phenoxazin-10-yl)dibenzo[f,h]quinoxaline (m-ATP-PXZ), 10-(4-(4,6-Diphenyl-1,3,5-triazin-2-yl)phenyl)-10H-phenoxazine (PXZ-TRZ), 10,10′-((6-Phenyl-1,3,5-triazine-2,4-diyl)bis(4,1-phenylene))bis(10H-phenoxazine (bis-PXZ-TRZ), 2,4,6-tris(4-(10H-phenoxazin-10-yl)phenyl)-1,3,5-triazine (tri-PXZ-TRZ), N1-(4-(4,6-diphenyl-1,3,5-triazin-2-yl)phenyl)-N1-(4-(diphenylamino)phenyl)-N4,N4-diphenylbenzene-1,4-diamine (DPA-TRZ), 2,3,5,6-teterkis(carbazol-9-yl)-1,4-dicyanobenzene (4CzTPN), 2,3,5,6-tetrakis(3,6-diphenylcarbazol-9-yl)-1,4-dicyanobenzene (4CzTPN-Ph), 2,3,5,6-tetra(9H-carbazol-9-yl)isonicotinonitrile (4CzCNPy), 1,3-bis[4-(10H-phenoxazin-10-yl)benzoyl]benzene (mPx2BBP), 10,10′-(sulfonylbis(4,1-phenylene))bis(5-phenyl-5,10-dihydrophenazine) (PPZ-DPS), 5,10-bis(4-(benzo[d]thiazol-2-yl)phenyl)-5,10-dihydrophenazine (DHPZ-2BTZ), 5,10-bis(4-(4,6-diphenyl-1,3,5-triazin-2-yl)phenyl)-5,10-dihydrophenazine (DHPZ-2TRZ) and/or 7,10-bis(4-(diphenylamino)phenyl)-2,3-dicyanopyrazino phenanathrene (TPA-DCPP). The following Chemical Formula 6 indicates some of the third compound DF that can be used with the second compound FD emitting red light.

In another exemplary aspect, the second compound FD may emit green light. In this case, the second compound FD may have PL λ_(max) between more than about 500 nm and about 560 nm, preferably between more than about 510 nm and about 550 nm, may have Abs. λ_(max) between more than about 490 nm and about 550 nm, preferably between more than about 500 nm and about 550 nm, and may have the structure of Chemical Formula 4 or 5. In this case, the third compound DF of the delayed fluorescent material may have PL λ_(max) between about more than 480 nm and about 560 nm, preferably between about more than 500 nm and about 550 nm.

As an example, when the second compound FD emits green light, the third compound DF appropriate for transferring exciton energy to the second compound FD may comprise, but is not limited to, a benzonitrile-based compound having a cyano moiety as an electron acceptor moiety, a triazine-based compound having a carbazole moiety and derivative thereof as an electron donor moiety and triazine moiety and derivative thereof as an electron acceptor moiety and/or a pyrimidine-based compound having a pyrimidine moiety and derivative thereof as an electron acceptor moiety.

For example, the third compound DF that can be used with the second compound FD emitting green light may comprise, but is not limited to, 9,9′,9″-(5-(4,6-diphenyl-1,3,5-triazin-2-yl)benzne-1,2,3-triyl)tris(9H-carbazole) (TczTrz), 9,9′,9″-(5-(4,6-diphenyl-1,3,5-triazin-2-yl)benzne-1,2,3-triyl)tris(3,6-dimethyl-9H-carbazole) (TmCzTrz), 9,9′-(2-3(3,6-dimethyl-9H-carbazol-9-yl)-5-(4,6-diphenyl-1,3,5-triazin-2-yl)-1,3-phenyiene)bis(9H-carbazole)(DCzmCzTrz), 2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile (4CzIPN), 2,4,5,6-tetrakis(3,6-dimethyl-9H-carbazol-9-yl)isophthalonitrile (m-4CzIPN), 2,4,5,6-tetrakis(3,6-di-tert-butyl-9H-carbazol-9-yl)isophthalonitrile (t-4CzIPN), 4,6-bis(4-(10H-phenoxazin-yl)phenyl)pyrimidine (PXZPM), 4,6-bis(4-(10H-phenoxazin-yl)phenyl)-2-methylpyrimidine (PXZMePM), 4,6-bis(4-(10H-phenoxazin-yl)phenyl)2-phenylpyrimidine (PXZPPM), 1,3,5-tri(phenoxazin-1-yl-pyridyl)benzene. The following Chemical Formula 7 indicates some of the third compound DF that can be used with the second compound FD emitting green light.

The first compound H in the EML 240A may be identical to the first compound in the EML 240. In this aspect, the contents of the first compound H may be larger than each of the contents of the second and third compounds FD and DF. Also, the contents of the third compound DF may be larger than the contents of the second compound FD. As an example, the contents of the first compound H may be larger than the contents of the third compound DF, and the contents of the third compound DF may be larger than the contents of the second compound FD.

In this case, the exciton energy can be transferred sufficiently from the third compound DF to the second compound FD. When the EML 240A comprises the first to third compounds, each contents of the second and third compounds DF and FD may be about 1 wt % to about 50 wt %. For example, the contents of the third compound DF in the EML 240A may be about 10 wt % to 50 wt %, preferably about 10 wt % to about 40 wt %, and the contents of the second compound FD in the EML 240A may be about 1 wt % to about 10 wt %.

The OLEDs in accordance with the previous aspects have a single-layered EML. Alternatively, an OLED in accordance with the present disclosure may include multiple-layered EML. FIG. 7 is a schematic cross-sectional view illustrating an OLED having a double-layered EML in accordance with another exemplary aspect of the present disclosure.

As illustrated in FIG. 7, the OLED D3 in accordance with this aspect includes first and second electrodes 310 and 330 facing each other and an emissive layer 320 having single emitting unit disposed between the first and second electrodes 310 and 330. In one exemplary aspect, the emissive layer 320 comprises an EML 340. Also, the emissive layer 320 comprises an HIL 350 and an HTL 360 each of which is disposed sequentially between the first electrode 310 and the EML 340, and an ETL 370 and an IL 380 each of which is disposed sequentially between the EML 340 and the second electrode 330. Alternatively, the emissive layer 320 may further comprise an EBL 365 disposed between the HTL 360 and the EML 340 and/or a HBL 375 disposed between the EML 340 and the ETL 370. The configuration of the first and second electrodes 310 and 330 as well as other layers except the EML 340 in the emissive layer 320 may be substantially identical to the corresponding electrodes and layers in the OLEDs D1 and D2.

The EML 340 includes a first EML (EML1) 342 and a second EML (EML2) 344. The EML1 342 is disposed between the EBL 365 and the HBL 375 and the EML2 344 is disposed between the EML1 342 and the HBL 375. One of the EML1 342 and the EML2 344 includes the second compound (Compound 2, second dopant) FD having the fluorescent property that is any organic compound having the structure of Chemical Formulae 1 to 5, and the other of the EML1 342 and the EML2 344 includes a fifth compound (Compound 5, first dopant) DF having the delayed fluorescent property. Hereinafter, the EML 340 where the EML1 342 comprises the second compound FD and the EML2 344 comprises the fifth compound DF will be explained.

The EML1 342 comprise the first compound (Compound 1, Host 1) H1 that may be the first host and the second compound FD having the fluorescent property that may be any organic compound having the structure of Chemical Formulae 1 to 5. While the organic compound having the structure of Chemical Formulae 1 to 5 has an advantage in terms of color purity due to its narrow FWHM, but its internal quantum efficiency is low because its triplet exciton cannot be involved in the luminescence process.

The EML2 344 comprises the fourth compound (Compound 4, Host 2) H2 that may be the second host and the fifth compound DF having the delayed fluorescent property. The energy level bandgap (ΔE_(ST) ^(DF)) between the excited singlet energy level S₁ ^(DF) and the excited triplet energy level T₁ ^(DF) of the fifth compound DF in the EML2 344 is equal to or less than about 0.3 eV (see, FIG. 5) so that triplet exciton energy of the fifth compound DF can be transferred upwardly to its own singlet exciton energy via RISC mechanism. While the fifth compound DF has high internal quantum efficiency, but it has poor color purity due to its wide FWHM.

However, in this exemplary aspect, the singlet exciton energy and the triplet exciton energy of the fifth compound DF having the delayed fluorescent property in the EML2 344 can be transferred to the second compound FD in the EML1 342 disposed adjacently to the EML2 344 by FRET mechanism, and the ultimate light emission occurs in the second compound FD within the EML1 342. In other words, the triplet exciton energy of the fifth compound DF is converted upwardly to its own singlet exciton energy in the EML2 344 by RISC mechanism. Then, the converted singlet exciton energy of the fifth compound DF is transferred to the singlet exciton energy of the second compound FD in the EML1 342 because the fifth compound DF has the excited singlet energy level S₁ ^(DF) higher than the excited singlet energy level S₁ ^(FD) of the second compound FD (see, FIG. 8).

The second compound FD in the EML1 342 can emit light using the triplet exciton energy as well as the singlet exciton energy. As described above, since Dexter energy transfer mechanism is limited in any organic compound having the structure of Chemical Formulae 1 to 5 owing to its molecular conformation, the singlet exciton energy is mainly transferred between the fifth and second compounds DF and FD via FRET mechanism. As the triplet exciton energy loss by Dexter mechanism is prevented, the OLED D3 can improved its quantum efficiency and enhance its color purity with narrow FWHM. Accordingly, as the singlet exciton energy generated at the fifth compound DF in the EML2 344 is efficiently transferred to the second compound FD in the EML1 342, the OLED D3 can implement hyper fluorescence. In this case, while the fifth compound DF having the delayed fluorescent property only acts as transferring exciton energy to the second compound FD, substantial light emission is occurred in the EML1 342 including the second compound FD.

Each of the EML1 342 and the EML2 344 includes the first compound H1 of the first host and the fourth compound H2 of the second host, respectively. In one exemplary aspect, each of the first and fourth compounds H1 and H2 may be the same as the first compound H described above, respectively.

In one exemplary aspect, the second compound FD in the EML1 342 may emit red light and may be any organic compound having the structure of Chemical Formula 2 or 3. In this case, the fifth compound DF of the delayed fluorescent material in the EML2 344 may have PL λ_(max) between about more than 500 nm and about 650 nm, preferably between about more than 550 nm and about 630 nm. As an example, the fifth compound DF may comprise, but is not limited to, a benzonitrile-based compound having a cyano moiety as an electron acceptor moiety, a triazine-based compound having a phenoxazine moiety, an aromatic or hetero aromatic amino moiety and derivative thereof as an electron donor moiety and a triazine moiety and derivative thereof as an electron acceptor moiety and/or a quinoxaline-based compound, for example, anyone having the structure of Chemical Formula 6.

In another exemplary aspect, the second compound FD in the EML1 342 may emit green light and may be any organic compound having the structure of Chemical Formula 4 or 5. In this case, the fifth compound DF of the delayed fluorescent material in the EML2 344 may have PL λ_(max) between about more than 480 nm and about 560 nm, preferably between about more than 500 nm and about 550 nm. As an example, the fifth compound DF may comprise, but is not limited to, a benzonitrile-based compound having a cyano moiety as an electron acceptor moiety, a triazine-based compound having a carbazole moiety and derivative thereof as an electron donor moiety and triazine moiety and derivative thereof as an electron acceptor moiety and/or a pyrimidine-based compound having a pyrimidine moiety and derivative thereof as an electron acceptor moiety, for example, anyone having the structure of Chemical Formula 7.

In one exemplary aspect, each of the contents of the first and fourth compounds H1 and H2 in the EML1 342 and the EML2 344 may be larger than the contents of the second and fifth compounds FD and DF in the same layer. Also, the contents of the fifth compound DF in the EML2 344 may be larger than the contents of the second compound FD in the EML1 342. In this case, exciton energy can be transferred sufficiently from the fifth compound DF to the second compound FD via FRET mechanism. As an example, the contents of the second compound FD in the EML1 342 may be, but is not limited to, about 1 wt % to about 50 wt %, preferably about 1 wt % to about 30 wt %. On the other hand, the contents of the fifth compound DF in the EML2 344 may be, but is not limited to, about 10 wt % to about 50 wt %, preferably about 10 wt % to about 40 wt %.

Now, we will explain the energy level relationships among the luminous material in the EML 340 with referring to FIG. 8. FIG. 8 is a schematic diagram illustrating luminous mechanism by energy level bandgap among luminous materials in accordance with another exemplary aspect of the present disclosure.

As illustrated in FIG. 8, the excited singlet energy level S₁ ^(m) of the first compound H1, which may be the first host, in the EML1 342 is higher than the excited singlet energy level S₁ ^(FD) of the second compound FD which may be the fluorescent material. Alternatively, the excited triplet energy level T₁ ^(m) of the first compound H1 may be higher than the excited singlet energy level T₁ ^(FD) of the second compound FD.

Also, each of the excited singlet energy level SP and excited triplet energy level T₁ ^(H2) of the fourth compound H2, which may be the second host, in the EML2 344 may be higher than each of the excited singlet energy level S₁ ^(DF) and the excited triplet energy level T₁ ^(DF) of the fifth compound DF having the delayed fluorescent property, respectively.

Moreover, the excited singlet energy level S₁ ^(DF) of the fifth compound DF in the EML2 344 is higher than the excited singlet energy level S₁ ^(FD) of the second compound FD in the EML1 342. Alternatively, the excited triplet energy level T₁ ^(DF) of the fifth compound DF in the EML2 344 is higher than the excited triplet energy level T₁ ^(FD) of the second compound FD in the EML1 342. When the luminous materials do not satisfy the requirements above, excitons may be quenched as non-radiation at each of the second compound FD having the fluorescent property and the fifth compound DF having the delayed fluorescent property or excitons cannot be transferred to the dopants from the hosts, and results in luminous efficiency reduction in the OLED D3.

The energy level bandgap between the excited singlet energy level S₁ ^(DF) and the excited triplet energy level T₁ ^(DF) of the fifth compound DF in the EML2 344 may be less than or equal to about 0.3 eV. Also, the energy level bandgap (|HOMO^(H)-HOMO^(DF)|) between the HOMO energy level (HOMO^(H)) of the first and/or fourth compounds H1 and/or H2 and the HOMO energy level (HOMO^(DF)) of the fifth compound DF, or the energy level bandgap (LUMO^(H)-LUMO^(DF) 1) between a LUMO energy level (LUMO^(H)) of the first and/or fourth compounds H1 and/or H2 and the LUMO energy level (LUMO^(DF)) of the fifth compound DF may be equal to or less than about 0.5 eV.

In another exemplary aspect, the first compound H1, which is included in the EML1 342 together with the second compound FD having the fluorescent property, may be the same material as the EBL 365. In this case, the EML1 342 may have an electron blocking function as well as an emission function. In other words, the EML1 342 can act as a buffer layer for blocking electrons. In one aspect, the EBL 365 may be omitted where the EML1 342 may be an electron blocking layer as well as an emitting material layer.

In another aspect, the EML1 342 may comprise the fourth compound H2 and the fifth compound DF having the delayed fluorescent property and the EML2 344 may comprise the first compound H1 and the second compound FD having the fluorescent property such as any organic compound having the structure of Chemical Formulae 1 to 6. In this case, the first compound H1 in the EML2 344 may be the same as the HBL 375. In this case, the EML2 344 may have a hole blocking function as well as an emission function. In other words, the EML2 344 can act as a buffer layer for blocking holes. In one aspect, the HBL 375 may be omitted where the EML2 344 may be a hole blocking layer as well as an emitting material layer.

An OLED having a triple-layered EML will be explained. FIG. 9 is a schematic cross-sectional view illustrating an OLED having a triple-layered EML in accordance with another exemplary aspect of the present disclosure. As illustrated in FIG. 9, the OLED D4 in this aspect comprises first and second electrodes 410 and 430 facing each other and an emissive layer 420 having a single emitting unit disposed between the first and second electrodes 410 and 430.

In one exemplary aspect, the emissive layer 420 having single emitting unit comprises a three-layered EML 440. The emissive layer 420 comprises an HIL 450 and an HTL 460 each of which is disposed sequentially between the first electrode 410 and the EML 440, and an ETL 470 and an EIL 480 each of which is disposed sequentially between the EML 440 and the second electrode 430. Alternatively, the emissive layer 420 may further comprise an EBL 465 disposed between the HTL 460 and the EML 440 and/or a HBL 475 disposed between the EML 440 and the ETL 470. The configurations of the first and second electrodes 410 and 430 as well as other layers except the EML 440 in the emissive layer 420 may be substantially identical to the corresponding electrodes and layers in the OLEDs D1, D2 and D3.

The EML 440 comprises a first EML (EML1) 442, a second EML (EML2) 444 and a third EML (EML3) 446. The EML1 442 is disposed between the EBL 465 and the HBL 475, the EML2 444 is disposed between the EBL 465 and the EML1 442 and the EML3 446 is disposed between the EML1 442 and the HBL 475.

Each of the EML1 442 and the EML3 446 comprises the second compound (Compound 2, dopant 2) FD1, which may be the first fluorescent material, and a seventh compound (Compound 7, third dopant) FD2, which may be a second fluorescent material, respectively. The EML2 444 comprises the fifth compound (Compound 5, first dopant) DF which may be the delayed fluorescent material. For example, each of the second and fifth compounds FD1 and FD2 may comprise any organic compound having the structure of Chemical Formulae 1 to 5. In addition, each of the EML1 442, EML2 444 and EML3 446 further includes the first compound (Compound 1, Host 1) H1, the fourth compound (Compound 4, Host 2) H2 and a sixth compound (Compound 6, Host 3) H3. Each of the first, fourth and sixth compounds H1, H2 and H3 may be the first to third hosts, respectively.

In accordance with this aspect, the singlet energy as well as the triplet energy of the fifth compound DF, i.e. the delayed fluorescent material in the EML2 444 can be transferred to the second and seventh compounds FD1 and FD2, i.e. the fluorescent materials each of which is included in the EML1 442 and EML3 446 disposed adjacently to the EML2 444 by FRET mechanism. Accordingly, the ultimate emission occurs in the second and seventh compounds FD1 and FD2 in the EML1 442 and the EML3 446.

In other words, the triplet exciton energy of the fifth compound DF having the delayed fluorescent property in the EML2 444 is converted upwardly to its own singlet exciton energy by RISC mechanism, then the singlet exciton energy of the fifth compound DF is transferred to the singlet exciton energy of the second and seventh compounds FD1 and FD2 in the EML1 442 and the EML3 446 because the fifth compound DF has the excited singlet energy level S₁ ^(DF) higher than each of the excited singlet energy levels S₁ ^(FD1) and S₁ ^(FD2) of the second and seventh compounds FD1 and FD2 (see, FIG. 10).

Since the second and seventh compounds FD1 and FD2 in the EML1 442 and EML3 446 can emit light using the singlet exciton energy and the triplet exciton energy derived from the fifth compound DF, the OLED D4 can improve its luminous efficiency. In addition, since each of the second and seventh compounds FD1 and FD2 having the fluorescent property each of which may be any organic compound having the structure of Chemical Formulae 1 to 5, has relatively narrow FWHM compared to the fifth compound DF, the OLED D4 can enhance its color purity. In this case, while the fifth compound DF having the delayed fluorescent property only acts as transferring exciton energy to the second and seventh compounds FD1 and FD2, substantial light emission is occurred in the EML1 442 and the EML3 446 including the second and seventh compounds FD1 and FD2.

Each of the EML1 442 to the EML3 446 includes the first compound H1 as the first host, the fourth compound H2 as the second host and the sixth compound H3 as the third host, respectively. In one exemplary aspect, each of the first, fourth and sixth compounds H1, H2 and H3 may be the same as the first compound H described above, respectively.

In one exemplary aspect, each of the second and seventh compounds FD1 and FD2 in the EML1 442 and the EML3 446 may emit red light and may be any organic compound having the structure of Chemical Formula 2 or 3. In this case, the fifth compound DF of the delayed fluorescent material in the EML2 444 may have PL λ_(max) between about more than 500 nm and about 650 nm, preferably between about more than 550 nm and about 630 nm, and may include anyone having the structure of Chemical Formula 7. In another exemplary aspect, each of the second and seventh compounds FD1 and FD2 in the EML1 442 and the EML3 446 may emit green light and may be any organic compound having the structure of Chemical Formula 4 or 5. In this case, the fifth compound DF of the delayed fluorescent material in the EML2 444 may have PL λ_(max) between about more than 480 nm and about 560 nm, preferably between about more than 500 nm and about 550 nm, and may include anyone having the structure of Chemical Formula 7.

In one exemplary aspect, each of the contents of the first, fourth and sixth compounds H1, H2 and H3 as the host in the EML1 442 to the EML3 446 may be larger than the contents of the second, fifth and seventh FD1, DF and FD2 compounds as the dopants in the same layer. Also, the contents of the fifth compound DF in the EML2 444 may be larger than the contents of each of the second and seventh compounds FD1 and FD2 in the EML1 442 and in the EML3 446. In this case, exciton energy can be transferred sufficiently from the fifth compound DF to the second and seventh compounds FD1 and FD2 via FRET mechanism. As an example, the contents of each of the second and seventh compounds FD1 and FD2 in the EML1 442 and in the EML3 446 may be, but is not limited to, about 1 wt % to about 50 wt %, preferably about 1 wt % to about 30 wt %. On the other hand, the contents of the fifth compound DF in the EML2 444 may be, but is not limited to, about 10 wt % to about 50 wt %, preferably about 10 wt % to about 40 wt %.

Now, we will explain the energy level relationships among the luminous material in the EML 440 with referring to FIG. 10. FIG. 10 is a schematic diagram illustrating luminous mechanism by energy level bandgap among luminous materials in accordance with another exemplary aspect of the present disclosure.

As illustrated in FIG. 10, the excited singlet energy level S₁ ^(H1) of the first compound H1, which may be the first host, in the EML1 442 is higher than the excited singlet energy level S₁ ^(FD1) of the second compound FD1 which may be the first fluorescent material. Also, the excited singlet energy level S₁ ^(DF) of the sixth compound H3, which may be the third host, in the EML3 446 is higher than the excited singlet energy level S₁ ^(FD2) of the seventh compound FD2 which may be the second fluorescent material. Alternatively, the excited triplet energy levels T₁ ^(H1) and T₁ ^(H2) of the first and sixth compounds H1 and H3 may be higher than each of the excited singlet energy levels T₁ ^(FD1) and T₁ ^(FD2) of the second and seventh compounds FD1 and FD2, respectively.

Also, each of the excited singlet energy level S₁ ^(H2) and excited triplet energy level T₁ ^(H2) of the fourth compound H2, which may be the second host, in the EML2 444 may be higher than each of the excited singlet energy level S₁ ^(DF) and the excited triplet energy level T₁ ^(DF) of the fifth compound having the delayed fluorescent property, respectively. In addition, each of the excited singlet energy levels S₁ ^(DF) and S₁ ^(DF) and the excited triplet energy levels T₁ ^(H1) and T₁ ^(H3) of the first and sixth compounds H1 and H3 in the EML1 442 and in the EML3 446 may be higher than each of excited singlet energy level S₁ ^(DF) and the excited triplet energy level T₁ ^(DF) of the fifth compound DF in the EML2 444.

Moreover, the excited singlet energy level S₁ ^(DF) of the fifth compound DF in the EML2 444 is higher than each of the excited singlet energy levels S₁ ^(DF) and S₁ ^(DF) of the second and seventh compounds FD1 and FD2 in the EML1 442 and in the EML3 446. Alternatively, the excited triplet energy level of the fifth compound DF in the EML2 444 is higher than each of the excited triplet energy levels T₁ ^(FD1) and T₁ ^(FD2) of the second and seventh compounds FD1 and FD2 in the EML1 442 and in the EML3 446.

In one exemplary aspect, the first compound H1, which is included in the EML1 442 together with the second compound FD1, may be the same material as the EBL 465. In this case, the EML1 442 may have an electron blocking function as well as an emission function. In other words, the EML1 442 can act as a buffer layer for blocking electrons. In one aspect, the EBL 465 may be omitted where the EML1 442 may be an electron blocking layer as well as an emitting material layer.

The sixth compound H3, which is included in the EML3 446 together with the seventh compound FD2, may be the same material as the HBL 475. In this case, the EML3 446 may have a hole blocking function as well as an emission function. In other words, the EML3 446 can act as a buffer layer for blocking holes. In one aspect, the HBL 475 may be omitted where the EML3 446 may be a hole blocking layer as well as an emitting material layer.

In still another exemplary aspect, the first compound H1 in the EML1 442 may be the same material as the EBL 455 and the sixth compound H3 in the EML3 446 may be the same material as the HBL 475. In this aspect, the EML1 442 may have an electron blocking function as well as an emission function, and the EML3 446 may have a hole blocking function as well as an emission function. In other words, each of the EML1 442 and the EML3 446 can act as a buffer layer for blocking electrons or hole, respectively. In one aspect, the EBL 465 and the HBL 475 may be omitted where the EML1 442 may be an electron blocking layer as well as an emitting material layer and the EML3 446 may be a hole blocking layer as well as an emitting material layer.

Synthesis Example 1: Synthesis of Compound 1-1 (1) Synthesis of Intermediate A-2

Compound A-1 (1 equivalent) was dissolved in tetrahydrofuran (THF), diisopropylethylamine (2 equivalents) was added into the solution, and then methoxymethylchloride (1.5 equivalents) was added slowly into the solution at 0° C. The mixture was reacted for 2 hours, and then the organic layer was extracted and purified with a column chromatography to give an intermediate A-2.

(2) Synthesis of Intermediate A-3

The intermediate A-2 (1 equivalent) was dissolved in THF, the temperature was cooled down to −78° C., and then 1.6 M n-butyllithium (1 equivalent) was added slowly into the solution. After stirring the solution for 1 hour, trimethylborate (4 equivalents) was added into the solution, the temperature was raised to room temperature, and then the mixture was reacted for 10 hours. Concentrated NH₄Cl aqueous solution was added into the solution, and then the solution was stirred again for 1 hour to complete the reaction. The organic layer was extracted and purified with a column chromatography to give an intermediate A-3.

(3) Synthesis of Intermediate A-5

The intermediate A-3 (1 equivalent), compound A-4 (0.8 equivalent), tetrakis(triphenylphosphine)palladium (0) (Pd(pph₃)₄, 0.02 equivalent) and Na₂CO₃ aqueous solution (4 equivalents) were dissolved in THF, and then the solution was refluxed for 20 hours to extract a crude product. The obtained crude product was purified with a column chromatography to give an intermediate A-5.

(4) Synthesis of Intermediate A-6

The intermediate A-5 (1 equivalent) and K₂CO₃ (2 equivalents) were dissolved in THF, and then the solution was refluxed for 15 hours to extract a crude product. The obtained crude product was purified with a column chromatography to give an intermediate A-6.

(5) Synthesis of Intermediate A-7

The intermediate A-6 (1 equivalent) was dissolved in THF, the temperature was cooled down to −78° C., and then 1.6 M n-butyllithium solution in hexane (1.5 equivalent) was added drop wisely into the solution. The temperature was raised to room temperature, and the temperature was cooled down to −78° C. again one hour later and then dimethylforamide (DMF, 3 equivalents) were added into the solution. After raising the temperature to room temperature, DI was added into the solution to quench the reaction, and then organic layer was extracted. The obtained crude product was purified with a column chromatography to give an intermediate A-7.

(6) Synthesis of Compound 1-1

The intermediate A-7 (1 equivalent) and compound B-1 (2.1 equivalents) were dissolved in dichloromethane, trifluoroacetic acid (6 drops) was added drop wisely into the solution, and then the solution was stirred for 8 hours. p-chloroaniline (1 equivalent) was added into the solution, and then the solution was stirred for 3 hours. Triethylamine (6 equivalents) was added into the solution, and then BF₃Et₂O (9 equivalents) was added drop wisely into the solution 20 minutes later. The mixture was reacted for 5 hours at room temperature to complete the reaction. The crude product was extracted and was purified with a column chromatography to give compound 1-1.

Synthesis Example 2: Synthesis of Compound 1-15 (1) Synthesis of Intermediate C-2

After wrapping the reactor with silver foil, compound C-1 (1 equivalent) dissolved in dichloromethane was added into the reactor, and then the temperature was cooled down to 0° C. Pyridine (1.1 equivalents) and acetyl chloride (0.8 equivalents) were added into the solution, and then the mixture was reacted for 2 hours. The organic layer was extracted, concentrated at low temperature, and then was re-crystallized to give an intermediate C-2.

(2) Synthesis of Intermediate C-4

After wrapping the reaction with silver foil, the intermediate C-2 (1 equivalent) and isopentyl nitrite (3 equivalents) dissolved in dichloromethane was added into the reactor, and then the solution was refluxed. Compound C-3 (1 equivalent) was injected slowly into the solution for 1 hour though a dropping funnel. After refluxing for 3 hours, the solution was cooled down to room temperature, the reactor was decompression, and then the crude product was purified with a column chromatography to give an intermediate C-4.

(3) Synthesis of Intermediate C-5

The intermediate C-4 was dissolved in dichloromethane, N-bromosuccinimide (1 equivalent) was added slowly into the solution, and then the mixture was reacted for 3 hours. After reaction was complete, the organic layer was extracted and purified with a column chromatography to give an intermediate C-5.

(4) Synthesis of Intermediate C-6

The intermediate C-5 was dissolved in THF, the temperature was cooled down to −78° C. and then 1.6 M n-butyllithium solution in hexane (1.5 equivalents) was added drip wisely into the solution. The temperature was raised to 0° C., and then was cooled down again to −78° C., and then DMF (3 equivalents) was added into the solution. After raising the temperature to room temperature, DI was added into the solution to quench the reaction, and then organic layer was extracted. The obtained crude product was purified with a column chromatography to give an intermediate C-6.

(5) Synthesis of Compound 1-15

The intermediate C-6 (1 equivalent) and compound B-1 (2.1 equivalents) were dissolved in dichloromethane, trifluoroacetic acid (6 drops) was added drop wisely into the solution, and then the solution was stirred for 8 hours. p-chloroaniline (1 equivalent) was added into the solution, and then the solution was stirred for 3 hours. Triethylamine (6 equivalents) was added into the solution, and then BF₃Et₂O (9 equivalents) was added drop wisely into the solution 20 minutes later. The mixture was reacted for 5 hours at room temperature to complete the reaction. The crude product was extracted and was purified with a column chromatography to give compound 1-15.

Synthesis Example 3: Synthesis of Compound 1-29 (1) Synthesis of Intermediate A-5-1

The intermediate A-3 (1 equivalent), compound A-4-1 (0.8 equivalents), Pd(pph₃)₄ (0.02 equivalent) and Na₂CO₃ aqueous solution (4 equivalents) were dissolved in THF, and then the solution was refluxed for 20 hours to extract a crude product. The obtained crude product was purified with a column chromatography to give an intermediate A-5-1.

(2) Synthesis of Intermediate A-6-1

The intermediate A-5-1 (1 equivalent) and K₂CO₃ (2 equivalents) were dissolved in THF, and then the solution was refluxed for 15 hours to extract a crude product. The obtained crude product was purified with a column chromatography to give an intermediate A-6-1.

(3) Synthesis of Intermediate A-7-1

The intermediate A-6-1 (1 equivalent) was dissolved in THF, the temperature was cooled down to −78° C., and then 1.6 M n-butyllithium solution in hexane (1.5 equivalent) was added drop wisely into the solution. The temperature was raised to room temperature, and the temperature was cooled down to −78° C. again one hour later and then DMF (3 equivalents) were added into the solution. After raising the temperature to room temperature, DI was added into the solution to quench the reaction, and then organic layer was extracted. The obtained crude product was purified with a column chromatography to give an intermediate A-7-1.

(4) Synthesis of Compound 1-29

The intermediate A-7-1 (1 equivalent) and compound B-2 (2.1 equivalents) were dissolved in dichloromethane, trifluoroacetic acid (6 drops) was added drop wisely into the solution, and then the solution was stirred for 8 hours. p-chloroaniline (1 equivalent) was added into the solution, and then the solution was stirred for 3 hours. Triethylamine (6 equivalents) was added into the solution, and then BF₃Et₂O (9 equivalents) was added drop wisely into the solution 20 minutes later. The mixture was reacted for 5 hours at room temperature to complete the reaction. The crude product was extracted and was purified with a column chromatography to give compound 1-29.

Synthesis Example 4: Synthesis of Compound 1-36 (1) Synthesis of Intermediate A-5-2

Compound A-3-1 (1 equivalent), compound A-4-2 (0.8 equivalents), Pd(pph₃)₄ (0.02 equivalent) and Na₂CO₃ aqueous solution (4 equivalents) were dissolved in a mixed solution of toluene/THF (5/1 volume %), and then the solution was refluxed for 2 hours to extract a crude product. The obtained crude product was purified with a column chromatography to give an intermediate A-5-2.

(2) Synthesis of Intermediate A-6-2

The intermediate A-5-2 (1 equivalent), KOH and Cu powder were added into the reactor, and then the mixture was reacted at 220° C. The obtained crude product was purified with a column chromatography to give an intermediate A-6-2.

(3) Synthesis of Intermediate A-7-2

The intermediate A-6-2 (1 equivalent) was dissolved in THF, the temperature was cooled down to −78° C., and then 1.6 M n-butyllithium solution in hexane (1.5 equivalent) was added drop wisely into the solution. The temperature was raised to room temperature, and the temperature was cooled down to −78° C. again one hour later and then DMF (3 equivalents) were added into the solution. After raising the temperature to room temperature, DI was added into the solution to quench the reaction, and then organic layer was extracted. The obtained crude product was purified with a column chromatography to give an intermediate A-7-2.

(4) Synthesis of Compound 1-36

The intermediate A-7-2 (1 equivalent) and compound B-2 (2.1 equivalents) were dissolved in dichloromethane, trifluoroacetic acid (6 drops) was added drop wisely into the solution, and then the solution was stirred for 8 hours. p-chloroaniline (1 equivalent) was added into the solution, and then the solution was stirred for 3 hours. Triethylamine (6 equivalents) was added into the solution, and then BF₃Et₂O (9 equivalents) was added drop wisely into the solution 20 minutes later. The mixture was reacted for 5 hours at room temperature to complete the reaction. The crude product was extracted and was purified with a column chromatography to give compound 1-36.

Synthesis Example 5: Synthesis of Compound 2-25 (1) Synthesis of Intermediate A-5-3

Compound A-3-2 (1 equivalent), compound A-4-3 (0.8 equivalents), Pd(pph₃)₄ (0.02 equivalent) and Na₂CO₃ aqueous solution (4 equivalents) were dissolved in THF, and then the solution was refluxed for 20 hours to extract a crude product. The obtained crude product was purified with a column chromatography to give an intermediate A-5-3.

(2) Synthesis of Intermediate A-6-3

The intermediate A-5-3 (1 equivalent) and K₂CO₃ (2 equivalents) were dissolved in THF, and then the solution was refluxed for 15 hours to extract a crude product. The obtained crude product was purified with a column chromatography to give an intermediate A-6-3.

(3) Synthesis of Intermediate A-7-3

The intermediate A-6-3 (1 equivalent) was dissolved in THF, the temperature was cooled down to −78° C., and then 1.6 M n-butyllithium solution in hexane (1.5 equivalent) was added drop wisely into the solution. The temperature was raised to room temperature, and the temperature was cooled down to −78° C. again one hour later and then DMF (3 equivalents) were added into the solution. After raising the temperature to room temperature, DI was added into the solution to quench the reaction, and then organic layer was extracted. The obtained crude product was purified with a column chromatography to give an intermediate A-7-3.

(4) Synthesis of Compound 2-25

The intermediate A-7-3 (1 equivalent) and compound B-2 (2.1 equivalents) were dissolved in dichloromethane, trifluoroacetic acid (6 drops) was added drop wisely into the solution, and then the solution was stirred for 8 hours. p-chloroaniline (1 equivalent) was added into the solution, and then the solution was stirred for 3 hours. Triethylamine (6 equivalents) was added into the solution, and then BF₃Et₂O (9 equivalents) was added drop wisely into the solution 20 minutes later. The mixture was reacted for 5 hours at room temperature to complete the reaction. The crude product was extracted and was purified with a column chromatography to give compound 2-25.

Synthesis Example 6: Synthesis of Compound 3-24 (1) Synthesis of Intermediate A-5-4

The intermediate A-3 (1 equivalent), compound A-4-4 (0.8 equivalents), Pd(pph₃)₄ (0.02 equivalent) and Na₂CO₃ aqueous solution (4 equivalents) were dissolved in THF, and then the solution was refluxed for 20 hours to extract a crude product. The obtained crude product was purified with a column chromatography to give an intermediate A-5-4.

(2) Synthesis of Intermediate A-6-4

The intermediate A-5-4 (1 equivalent) and K₂CO₃ (2 equivalents) were dissolved in THF, and then the solution was refluxed for 15 hours to extract a crude product. The obtained crude product was purified with a column chromatography to give an intermediate A-6-4.

(3) Synthesis of Intermediate A-7-4

The intermediate A-6-4 (1 equivalent) was dissolved in THF, the temperature was cooled down to −78° C., and then 1.6 M n-butyllithium solution in hexane (1.5 equivalent) was added drop wisely into the solution. The temperature was raised to room temperature, and the temperature was cooled down to −78° C. again one hour later and then DMF (3 equivalents) were added into the solution. After raising the temperature to room temperature, DI was added into the solution to quench the reaction, and then organic layer was extracted. The obtained crude product was purified with a column chromatography to give an intermediate A-7-4.

(4) Synthesis of Compound 3-24

The intermediate A-7-4 (1 equivalent) and compound B-2 (2.1 equivalents) were dissolved in dichloromethane, trifluoroacetic acid (6 drops) was added drop wisely into the solution, and then the solution was stirred for 8 hours. p-chloroaniline (1 equivalent) was added into the solution, and then the solution was stirred for 3 hours. Triethylamine (6 equivalents) was added into the solution, and then BF₃Et₂O (9 equivalents) was added drop wisely into the solution 20 minutes later. The mixture was reacted for 5 hours at room temperature to complete the reaction. The crude product was extracted and was purified with a column chromatography to give compound 3-24.

Experimental Example 1: Measurement of Absorption and Luminescence Wavelength

Physical properties such as the maximum absorption wavelength (Abs. λ_(max)), the maximum photoluminescence wavelength (PL λ_(max)), stokes shift between the Abs. λ_(max) and the PL λ_(max), and the photoluminescence quantum efficiency (PLQY) for each of the compounds 1-1, 1-15, 2-25 and 3-24 synthesized in the Synthesis Examples 1, 2, 5 and 6 as well as the red fluorescent compound Ref. 1 and the green fluorescent compound Ref. 2 as indicated below for comparison. Table 1 below indicates the measurement results and also indicates PL λ_(max) of the yellow-green delayed fluorescent material 4CzTPN and the green delayed fluorescent material 4CzIPN.

[Reference compound]

TABLE 1 Physical Property of Organic Compound Abs. λ_(max) ^(a) PL λ_(max) ^(b) Stokes PLQY^(c) Compound (nm) (nm) Shfit (%) Ref. 1 563 600 37 35 1-1  570 604 34 85 1-15 581 615 34 96 2-25 589 625 36 90 4CzTPN — 575 — — Ref. 2 504 514 10 57 3-24 509 524 15 91 4CzIPN — 540 — — ^(a)measured using UV-Vis spectroscopy in solution state of 10⁻⁵M in toluene; ^(b)measured usinng fluorescence spectroscopy in solution state of 10⁻⁵M in toluene; ^(c)measured uinsg Quantarus-QY (Hamamatsu, Japan) in soultion state of 10⁻⁵M in toluene;

As illustrated in Table 1, the organic compound synthesized in the Synthesis Examples had improved PLQY compared to the Ref. 1 and Ref. 2 compounds. Particularly, compounds 1-1, 1-15 and 2-25 has PL λ_(max) of red wavelength ranges and has Abs. λ_(max) having large overlapping area with the PL λ_(max) of 4CzTPN, i.e. 575 nm. On the other hand, compound 3-24 has PL λ_(max) of green wavelength ranges and has Abs. λ_(max) having large overlapping area with the PL λ_(max) of 4CzIPN, i.e. 540 nm. It was expected that OLED can implement hyper fluorescence having excellent color purity and improved luminous efficiency when an EML includes a delayed fluorescent material of which PL λ_(max) has large overlapped area with the PL λ_(max) of the compound synthesized in the Synthesis Examples.

Example 1 (Ex. 1): Fabrication of OLED

An OLED in which the Compound 1-1 is applied as an ultimate dopant into an EML was fabricated. An ITO (50 nm) attached glass substrate was washed ozone and was loaded into the vapor system, and then was transferred to a vacuum deposition chamber in order to deposit other layers on the substrate. An organic layer was deposited by evaporation by a heated boat under 10⁻⁶ torr in the following order.

A HIL (HAT-CN; 50 Å); a HTL (NPB, 550 Å); an EBL (3,6-bis(N-carbazolyl)-N-phenyl carbazole; 100 Å); an EML (mCBP (host): 5CzTPN: compound 1−1=70:29:1 by weight; 250 Å); a HBL (mCBP; 100 Å); an ETL (TPBi; 250 Å); an EIL (LiF; 10 Å); and a cathode (Al; 1000 Å).

And then, cappling layer (CPL) was deposited over the cathode and the device was encapsualted by glass. After deposition of emissve layer and the cathode, the OLED was transferred from the depostion chamber to a dry box for film formation, followed by encapsulation using UV-curable epoxy resin and moisture getter.

Examples 2-3 (Ex. 2-3): Fabrication of OLED

An OLED was fabricated using the same materials as Example 1, except that Compound 1-15 (Ex. 2) or Compound 2-25 (Ex. 3) was applied into the EML as the ultimate dopant instead of the Compound 1-1.

Comparative Example 1 (Ref 1): Fabrication of OLED

An OLED was fabricated using the same materials as Example 1, except that Ref. 1 Compound was applied into the EML as the ultimate dopant instead of the Compound 1-1.

Examples 4 (Ex. 4): Fabrication of OLED

An OLED was fabricated using the same materials as Example 1, except that Compound 3-24 as the ultimate dopant instead of Compound 1-1 and green delayed fluorescent material 4CzIPN as the delayed fluorescent material instead of 4CzTPN were applied into the EML.

Comparative Example 2 (Ref 2): Fabrication of OLED

An OLED was fabricated using the same materials as Example 4, except that Ref. 2 Compound (Ref 1) was applied into the EML as the ultimate dopant instead of the Compound 3-24.

Experimental Example 2: Measurement of Luminous Properties of OLED

Each of the OLED fabricated by Ex. 1-4 and Ref. 1-2 was connected to an external power source and then luminous properties for all the diodes were evaluated using a constant current source (KEITHLEY) and a photometer PR650 at room temperature. In particular, driving voltage (V), maximum External Quantum Efficiency (EQE_(max), %), CIE color coordinates, maximum electroluminescence wavelength (EL λ_(max), nm) and FWHM (nm) at a current density of 10 mA/cm² were measured. The results thereof are shown in the following Table 2.

TABLE 2 Luminous Properties of OLED Sample Dopant V EQE_(max) CIE (x, y) EL_(max) FWHM Ref. 1 Ref. 1 5.8 9.4 (0.598, 0.382) 604 44 Ex. 1 1-1  5.2 12.5 (0.639, 0.355) 610 40 Ex. 2 1-25 5.1 15.3 (0.653, 0.345) 618 38 Ex. 3 2-25 5.1 13.8 (0.674, 0.323) 631 42 Ref 2 Ref. 2 5.1 3.9 (0.301, 0.640) 524 32 Ex. 4 3-24 3.9 13.1 (0.313, 0.645) 526 36

As indicated in Table 2, compared to the OLED in Ref. 1, the OLEDs in Ex. 1-3 lowered their driving voltages up to 12.1%, enhanced their EQE_(max) up to 62.8%, reduced their FWHM slightly, which indicates an increased color purity, and emitted deep red color. In addition, compared to the OLED in Ref. 2, the OLEDs in Ex. 4 lowered its driving voltage 23.5% and enhanced its EQE_(max) 235.9%. It is possible to manufacture an OLED and an organic light emitting device having the OLED each of which lowers its driving voltages, enhances its luminous efficiency and color purity.

It will be apparent to those skilled in the art that various modifications and variations can be made in the present disclosure without departing from the scope of the invention. Thus, it is intended that the present disclosure cover the modifications and variations of the present disclosure provided they come within the scope of the appended claims. 

What is claimed is:
 1. An organic compound having the following structure of Chemical Formula 1:

wherein each of R₁ to R₆ is independently selected from the group consisting of hydrogen, an unsubstituted or substituted C₁-C₂₀ alkyl group, an unsubstituted or substituted C₁-C₂₀ alkoxy group, an unsubstituted or substituted C₁-C₂₀ alkyl amino group, an unsubstituted or substituted C₆-C₃₀ aromatic group and an unsubstituted or substituted C₃-C₃₀ hetero aromatic group, or two adjacent groups among R₁ to R₆ form a C₆-C₂₀ fused aromatic ring or a C₃-C₂₀ fused hetero aromatic ring; each of A₁ to A₄ is independently CR₈ or nitrogen (N), wherein at least one of A₁ to A₄ is nitrogen; each of R₇ and R₈ is independently hydrogen, an unsubstituted or substituted C₁-C₁₀ alkyl group, an unsubstituted or substituted C₆-C₃₀ aromatic group or an unsubstituted or substituted C₃-C₃₀ hetero aromatic group; each of X₁ and X₂ is independently halogen, a nitrile group, a C₁-Cao alkyl group or a C₁-Cao halo alkyl group; and X₃ is oxygen (O) or sulfur (S).
 2. The organic compound of claim 1, wherein at least four of R₁ to R₆ in Chemical Formula 1 is independently selected from the group consisting of an unsubstituted or substituted C₆-C₃₀ aryl group and an unsubstituted or substituted C₃-C₃₀ hetero aryl group, and any one of A₁ to A₄ is nitrogen.
 3. The organic compound of claim 1, wherein the organic compound has a maximum photoluminescence peak between more than about 560 nm and about 670 nm and has a maximum absorption peak between more than about 550 nm and about 650 nm.
 4. The organic compound of claim 3, wherein the organic compound includes anyone having the following structure of Chemical Formula 2:


5. The organic compound of claim 3, wherein the organic compound includes anyone having the following structure of Chemical Formula 3:


6. The organic compound of claim 1, wherein the organic compound has a maximum photoluminescence peak between more than about 500 nm and about 560 nm and has a maximum absorption peak between more than about 490 nm and about 550 nm.
 7. The organic compound of claim 1, wherein the organic compound includes anyone having the following structure of Chemical Formula 4:


8. The organic compound of claim 1, wherein the organic compound includes anyone having the following structure of Chemical Formula 5:


9. An organic light emitting diode, comprising: a first electrode; a second electrode facing the first electrode; and a first emitting material layer disposed between the first and second electrodes, wherein the first emitting material layer comprises an organic compound having the following structure of Chemical Formula 1:

wherein each of R₁ to R₆ is independently selected from the group consisting of hydrogen, an unsubstituted or substituted C₁-C₂₀ alkyl group, an unsubstituted or substituted C₁-C₂₀ alkoxy group, an unsubstituted or substituted C₁-C₂₀ alkyl amino group, an unsubstituted or substituted C₆-C₃₀ aromatic group and an unsubstituted or substituted C₃-C₃₀ hetero aromatic group, or two adjacent groups among R₁ to R₆ form a C₆-C₂₀ fused aromatic ring or a C₃-C₂₀ fused hetero aromatic ring; each of A₁ to A₄ is independently CR₈ or nitrogen (N), wherein at least one of A₁ to A₄ is nitrogen; each of R₇ and R₈ is independently hydrogen, an unsubstituted or substituted C₁-C₁₀ alkyl group, an unsubstituted or substituted C₆-C₃₀ aromatic group or an unsubstituted or substituted C₃-C₃₀ hetero aromatic group; each of X₁ and X₂ is independently halogen, a nitrile group, a C₁-Cao alkyl group or a C₁-Cao halo alkyl group; and X₃ is oxygen (O) or sulfur (S).
 10. The organic light emitting diode of claim 9, wherein at least four of R₁ to R₆ in Chemical Formula 1 is independently selected from the group consisting of an unsubstituted or substituted C₆-C₃₀ aryl group and an unsubstituted or substituted C₃-C₃₀ hetero aryl group, and any one of A₁ to A₄ is nitrogen.
 11. The organic light emitting diode of claim 9, wherein the first emitting material layer comprises a first compound and a second compound, wherein an excited singlet energy level of the first compound is higher than an excited singlet energy level of the second compound, and wherein the second compound comprises the organic compound.
 12. The organic light emitting diode of claim 9, wherein the first emitting material layer comprises a first compound, a second compound and a third compound, and wherein the second compound comprises the organic compound.
 13. The organic light emitting diode of claim 12, wherein the second compound has a maximum photoluminescence peak between more than about 560 nm and about 670 nm and has a maximum absorption peak between more than about 550 nm and about 650 nm, and the third compound has a maximum photoluminescence peak between more than about 500 nm and about 650 nm.
 14. The organic light emitting diode of claim 12, wherein the second compound has a maximum photoluminescence peak between more than about 500 nm and about 560 nm and has a maximum absorption peak between more than about 490 nm and about 550 nm, and the third compound has a maximum photoluminescence peak between more than about 480 nm and about 560 nm.
 15. The organic light emitting diode of claim 12, wherein an energy level bandgap between an excited singlet energy level and an excited triplet energy level of the third compound is about 0.3 eV or less, and wherein an excited singlet energy level of the second compound is lower than an excited singlet energy level of the third compound.
 16. The organic light emitting diode of claim 11, further comprises a second emitting material layer disposed between the first electrode and the first emitting material layer or between the first emitting material layer and the second electrode, and wherein the second emitting material layer comprises a fourth compound and a fifth compound.
 17. The organic light emitting diode of claim 16, wherein the second compound has a maximum photoluminescence peak between more than about 560 nm and about 670 nm and has a maximum absorption peak between more than about 550 nm and about 650 nm, and the fifth compound has a maximum photoluminescence peak between more than about 500 nm and about 650 nm.
 18. The organic light emitting diode of claim 16, wherein the second compound has a maximum photoluminescence peak between more than about 500 nm and about 560 nm and has a maximum absorption peak between more than about 490 nm and about 550 nm, and the fifth compound has a maximum photoluminescence peak between more than about 480 nm and about 560 nm.
 19. The organic light emitting diode of claim 16, wherein an energy level bandgap between an excited singlet energy level and an excited triplet energy level of the fifth compound is about 0.3 eV or less, and wherein an excited singlet energy level of the second compound is lower than an excited singlet energy level of the fifth compound.
 20. The organic light emitting diode of claim 16, further comprises a third emitting material layer disposed oppositely to the first emitting material layer with respect to the second emitting material layer, and wherein the third emitting material layer comprises a sixth compound and a seventh compound.
 21. The organic light emitting diode of claim 20, wherein an excited singlet energy level of the sixth compound is higher than an excited singlet energy level of the seventh compound, and wherein the seventh compound comprises the organic compound.
 22. An organic light emitting device, comprising: a substrate; and an organic light emitting diode of claim 9 over the substrate. 